@prefix dcterms: . @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:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_head { this: np:hasAssertion dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_assertion; np:hasProvenance dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_provenance; np:hasPublicationInfo dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_publicationInfo; a np:Nanopublication . dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_assertion a np:Assertion . dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_provenance a np:Provenance . dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_publicationInfo a np:PublicationInfo . } dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_assertion { miriam-gene:367 a ncit:C16612 . lld:C0039585 a ncit:C7057 . dgn-gda:DGN250e981667bd0973a5bb91895d5a5b5d sio:SIO_000628 miriam-gene:367, lld:C0039585; a sio:SIO_001122 . } dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_provenance { dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_assertion dcterms:description "[Subjects with androgen insensitivity syndromes (AIS) are characterized by a 46, XY karyotype, presence of testes, normal or elevated androgen levels in blood, and impairment of the usual response to androgens associated with various aberrations of male differentiation and virilization ranging from slightly undervirilized men to phenotypic females.]. 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:10221770; prov:wasDerivedFrom dgn-void:uniprot-2016; 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-2016 pav:importedOn "2016-01-25"^^xsd:date . } dgn-np:NP147.RAFdKEj3aFoKpUybjlg6h0P5DZ97m1ujrn87ukkJnFAjk130_publicationInfo { this: dcterms:created "2016-05-13T12:41:50+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }