@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 dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_head { this: np:hasAssertion dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_assertion; np:hasProvenance dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_provenance; np:hasPublicationInfo dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_publicationInfo; a np:Nanopublication . dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_assertion a np:Assertion . dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_provenance a np:Provenance . dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_assertion { miriam-gene:7531 a ncit:C16612 . lld:C0206630 a ncit:C7057 . dgn-gda:DGNde4208bf0928a2ccdd59dbab3ad31aee sio:SIO_000628 miriam-gene:7531, lld:C0206630; a sio:SIO_001121 . } dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_provenance { dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_assertion dcterms:description "[Collectively, these findings suggest that abnormality in the loci of YWHAE, FAM22A and FAM22B, which are known to be associated with oncogenesis of endometrial stromal sarcoma, may contribute to the development of uterine angiosarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:24125656; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1119199.RAchTcVhXliLQL52QZ7x9cXgdRQlzgEY96qxZX2EPXLN0130_publicationInfo { this: dcterms:created "2016-05-13T12:50:13+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" . }