add ORCID to mappings (#6494)

* add ORCID to mappings * add ORCID
monarch-initiative · Jul 25, 2023 · e0d9734 · e0d9734
1 parent 94f74b8
commit e0d9734
Showing 1 changed file with 8 additions and 8 deletions.
diff --git a/src/ontology/mondo-edit.obo b/src/ontology/mondo-edit.obo
@@ -124594,7 +124594,7 @@ synonym: "Alzheimer disease, protection against" RELATED [OMIM:104300]
 synonym: "Alzheimer disease, susceptibility to" RELATED [OMIM:104300, OMIM:genemap2]
 synonym: "early-onset familial form of Alzheimer disease" BROAD [GARD:0009465]
 synonym: "presenile and senile dementia" RELATED [OMIM:104300]
-xref: DECIPHER:48 {source="MONDO:relatedTo"}
+xref: DECIPHER:48 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:relatedTo"}
 xref: DOID:0080348 {source="MONDO:equivalentTo"}
 xref: GARD:0009465 {source="MONDO:equivalentTo"}
 xref: MESH:C536594 {source="MONDO:equivalentTo"}
@@ -265340,7 +265340,7 @@ synonym: "chromosome 16p12.2-p11.2 deletion syndrome, isolated cases" EXACT [OMI
 synonym: "Del(16)(p11.2p12.2)" EXACT [Orphanet:261211]
 synonym: "monosomy 16p11.2-p12.2" EXACT [Orphanet:261211]
 synonym: "monosomy 16p11.2p12.2" EXACT [Orphanet:261211]
-xref: DECIPHER:68 {source="MONDO:equivalentTo"}
+xref: DECIPHER:68 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo"}
 xref: DOID:0060400 {source="MONDO:equivalentTo"}
 xref: ICD10CM:Q93.5 {source="DOID:0060400", source="Orphanet:261211", source="Orphanet:261211/attributed", source="Orphanet:261211/ntbt"}
 xref: OMIM:613604 {source="DOID:0060400", source="MONDO:equivalentTo", source="Orphanet:261211", source="Orphanet:261211/e"}
@@ -309419,13 +309419,13 @@ synonym: "2p21 deletion syndrome" EXACT [Orphanet:163693]
 synonym: "2p21 microdeletion syndrome" EXACT [DECIPHER:87]
 synonym: "Del(2)(p21)" EXACT [Orphanet:163693]
 synonym: "monosomy 2p21" EXACT [Orphanet:163693]
-xref: DECIPHER:87 {source="MONDO:equivalentTo"}
+xref: DECIPHER:87 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo"}
 xref: ICD10CM:Q93.5 {source="Orphanet:163693/attributed", source="Orphanet:163693/ntbt", source="Orphanet:163693"}
 xref: Orphanet:163693 {source="MONDO:equivalentTo"}
 xref: SCTID:719652007 {source="MONDO:equivalentTo"}
 xref: UMLS:C4304537 {source="MONDO:equivalentTo"}
 xref: UMLS:CN199952 {source="MONDO:equivalentTo"}
-is_a: MONDO:0016884 {source="https://orcid.org/0000-0001-5208-3432"} ! partial deletion of the short arm of chromosome 2
+is_a: MONDO:0016884 {source="https://orcid.org/0000-0001-5208-3432", source="https://orcid.org/0009-0001-6494-4831"} ! partial deletion of the short arm of chromosome 2
 intersection_of: MONDO:0000761 ! syndrome caused by partial chromosomal deletion
 intersection_of: disease_arises_from_structure CHR:9606-chr2p21 ! 2p21 (Human)
 relationship: excluded_subClassOf MONDO:0011669 {source="Orphanet:163693"} ! hypotonia-cystinuria syndrome
@@ -326367,7 +326367,7 @@ subset: gard_rare {source="GARD:0010304"}
 subset: ordo_malformation_syndrome {source="Orphanet:251076"}
 synonym: "dup(8)(p23.1p23.1)" EXACT [Orphanet:251076]
 synonym: "trisomy 8p23.1" EXACT [Orphanet:251076]
-xref: DECIPHER:85 {source="MONDO:equivalentTo"}
+xref: DECIPHER:85 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo"}
 xref: GARD:0010304 {source="MONDO:equivalentTo"}
 xref: Orphanet:251076 {source="MONDO:equivalentTo"}
 xref: SCTID:765140006 {source="MONDO:equivalentTo"}
@@ -329458,8 +329458,8 @@ synonym: "16p11.2 microduplication syndrome" EXACT [DECIPHER:78, Orphanet:261204
 synonym: "16p11.2-p12.2 microduplication syndrome" EXACT [DECIPHER:96]
 synonym: "dup(16)(p11.2p12.2)" EXACT [Orphanet:261204]
 synonym: "trisomy 16p11.2p12.2" EXACT [Orphanet:261204]
-xref: DECIPHER:78 {source="MONDO:equivalentTo"}
-xref: DECIPHER:96 {source="MONDO:equivalentTo"}
+xref: DECIPHER:78 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo"}
+xref: DECIPHER:96 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="MONDO:preferredExternal"}
 xref: Orphanet:261204 {source="MONDO:equivalentTo"}
 xref: SCTID:733518000 {source="MONDO:equivalentTo"}
 xref: UMLS:C4518821 {source="MONDO:equivalentTo"}
@@ -379905,7 +379905,7 @@ synonym: "9qSTDS" EXACT [Orphanet:96147]
 synonym: "Kleefstra syndrome due to 9q subtelomeric deletion" EXACT [Orphanet:96147]
 synonym: "Kleefstra syndrome due to del(9)(q34)" EXACT [Orphanet:96147]
 synonym: "Kleefstra syndrome due to monosomy 9q34" EXACT [Orphanet:96147]
-xref: DECIPHER:52 {source="MONDO:equivalentTo"}
+xref: DECIPHER:52 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo"}
 xref: ICD10CM:Q87.8 {source="Orphanet:96147", source="Orphanet:96147/attributed", source="Orphanet:96147/ntbt"}
 xref: Orphanet:96147 {source="MONDO:equivalentTo"}
 xref: UMLS:C0795833 {source="Orphanet:96147"}