@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:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_head { this: np:hasAssertion dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_assertion; np:hasProvenance dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_provenance; np:hasPublicationInfo dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_publicationInfo; a np:Nanopublication . dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_assertion a np:Assertion . dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_provenance a np:Provenance . dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_publicationInfo a np:PublicationInfo . } dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_assertion { miriam-gene:7030 a ncit:C16612 . lld:C0007134 a ncit:C7057 . dgn-gda:DGN1e820cda90a91f237f1e4c8e75655448 sio:SIO_000628 miriam-gene:7030, lld:C0007134; a sio:SIO_001121 . } dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_provenance { dgn-np:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_assertion dcterms:description "[We analyzed a series of sporadic type 1 and type 2 PRCC cases for MET mutations, TFE3 rearrangements, and allelic imbalance (AI) on 3p, 6, 7q, 9p, 11, 13q, 14q, 17q, 18, 20q, and 21q and compared selected results with a series of conventional renal cell carcinomas.]. 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:12213728; 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:NP366946.RAy_PqKUtpaiyDq9qP5uvKQI0_LXOwUUVKpsF5Y2_lonI130_publicationInfo { this: dcterms:created "2016-05-13T12:44:31+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" . }