@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:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_head { this: np:hasAssertion dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_assertion; np:hasProvenance dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_provenance; np:hasPublicationInfo dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_publicationInfo; a np:Nanopublication . dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_assertion a np:Assertion . dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_provenance a np:Provenance . dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_publicationInfo a np:PublicationInfo . } dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_assertion { miriam-gene:7515 a ncit:C16612 . lld:C2939419 a ncit:C7057 . dgn-gda:DGN714ba317cc659cecc9026686b28cb522 sio:SIO_000628 miriam-gene:7515, lld:C2939419; a sio:SIO_001121 . } dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_provenance { dgn-np:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_assertion dcterms:description "[Our conclusions are as follows: (1) renal oncocytomas may have intravascular extension to the branches of the renal vein; (2) renal oncocytomas with intravascular extension to the branches of the renal vein have the same morphological, immunohistochemical, and cytogenetic findings as have their counterparts without evidence of intravascular invasion; (3) the absence of metastases suggests an overall benign behavior of this tumor, but this has to be substantiated by further studies with a long-term follow-up; and (4) in a renal tumor with granular cytoplasm showing renal vein extension, it is necessary to carefully exclude renal cell carcinomas such as chromophobe RCC, oncocytic variant of papillary RCC, and granular variant of clear cell RCC.]. 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:18066590; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP868417.RA4o7czjKGE2C7v7o3uZyq8GWsw8Nb1hdlyw32-Nbhy7I130_publicationInfo { this: dcterms:created "2014-10-02T12:40:50+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }