@prefix dc: .
@prefix orcid: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix eco: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_head {
this: np:hasAssertion dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion;
np:hasProvenance dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance;
np:hasPublicationInfo dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_publicationInfo;
a np:Nanopublication .
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion a np:Assertion .
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance a np:Provenance .
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion {
miriam-gene:268 a ncit:C16612 .
lld:C1849930 a ncit:C7057 .
dgn-gda:DGN5048374e561f254d485d59aafbac7c0f sio:SIO_000628 miriam-gene:268, lld:C1849930;
a sio:SIO_001122 .
}
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_provenance {
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_assertion dc:description
"[The persistent mA1/4llerian duct syndrome, characterized by the lack of regression of mA1/4llerian derivatives, uterus and tubes in otherwise normally masculinized males, is a genetically transmitted disorder implicating either anti-mA1/4llerian hormone (AMH), a member of the transforming growth factor-beta superfamily, or its type II receptor, a serine/threonine kinase homologous to the receptors of other members of the transforming growth factor-beta superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
wi:evidence dgn-void:source_evidence_curated;
sio:SIO_000772 miriam-pubmed:8872466;
prov:wasDerivedFrom dgn-void:uniprot-20150221;
prov:wasGeneratedBy eco:ECO_0000218 .
dgn-void:source_evidence_curated a eco:ECO_0000205;
rdfs:comment "Gene-disease associations manually curated."@en;
rdfs:label "DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20150221 pav:importedOn "2015-02-21"^^xsd:date .
}
dgn-np:NP957.RAZu_YelwKo-VToLGEd2CKuusJGptSaQ-rVc77mqYtl6E130_publicationInfo {
this: dc:created "2015-08-25T14:37:42+02:00"^^xsd:dateTime;
dc:rights ;
dc:rightsHolder dgn-void:IBIGroup;
dc:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetv3.0rdf;
pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
pav:createdBy orcid:0000-0003-0169-8159;
pav:version "v3.0.0.0" .
dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}