@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:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_head { this: np:hasAssertion dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_assertion; np:hasProvenance dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_provenance; np:hasPublicationInfo dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_publicationInfo; a np:Nanopublication . dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_assertion a np:Assertion . dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_provenance a np:Provenance . dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_publicationInfo a np:PublicationInfo . } dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_assertion { miriam-gene:5728 a ncit:C16612 . lld:C0027627 a ncit:C7057 . dgn-gda:DGN24dc7f533665a3ebc111ff23e59bb27f sio:SIO_000628 miriam-gene:5728, lld:C0027627; a sio:SIO_001121 . } dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_provenance { dgn-np:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_assertion dcterms:description "[Except for true de novo mutations in 4 cases (affecting SYNE1, CTNNB1, TP53, and PTEN), all remaining cases (84.4%) shared the genetic lesions of the primary tumors with all investigated metastases irrespective of the site of metastasis or time lapse between primary tumor resection and the occurrence of metastatic spread.]. 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:25786087; 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:NP1272150.RAOg-OJ1qHG19mjdGoqi77ZtCTsT9uBPnviOOIYFmxWtE130_publicationInfo { this: dcterms:created "2016-05-13T12:51:23+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" . }