@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:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_head { this: np:hasAssertion dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_assertion; np:hasProvenance dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_provenance; np:hasPublicationInfo dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_publicationInfo; a np:Nanopublication . dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_assertion a np:Assertion . dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_provenance a np:Provenance . dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_publicationInfo a np:PublicationInfo . } dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0919267 a ncit:C7057 . dgn-gda:DGNeafe66b8d5d686f7034dbc95a4306aba sio:SIO_000628 miriam-gene:7157, lld:C0919267; a sio:SIO_001121 . } dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_provenance { dgn-np:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_assertion dcterms:description "[Specific emphasis is placed on genetic alterations and the prevalence of TP53 (p53) gene alterations in the distinct biological ovarian tumors (benign, borderline, and malignant) and histological subtypes (serous, mucinous, endometrioid, clear cell), as well as in BRCA1-associated hereditary ovarian cancer.]. 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:12619114; 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:NP385857.RAw6Vol1s_o-hTL_1uRjLR74dRUzrOTKUrTm7LchsSz50130_publicationInfo { this: dcterms:created "2016-05-13T12:44:40+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" . }