@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:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_head { this: np:hasAssertion dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_assertion; np:hasProvenance dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_provenance; np:hasPublicationInfo dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_publicationInfo; a np:Nanopublication . dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_assertion a np:Assertion . dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_provenance a np:Provenance . dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_publicationInfo a np:PublicationInfo . } dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_assertion { miriam-gene:56955 a ncit:C16612 . lld:C0001418 a ncit:C7057 . dgn-gda:DGNb72b890f3a3e32983c1f36b29fb9ee3a sio:SIO_000628 miriam-gene:56955, lld:C0001418; a sio:SIO_001121 . } dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_provenance { dgn-np:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_assertion dcterms:description "[TP53 mutations were identified in 9.1% of intermediate-grade IPMNs (2 of 22), 17.8% of PanIN-2 (8 of 45), 38.1% of high-grade IPMNs (8 of 21), 47.6% of PanIN-3 (10 of 21), and 75% of invasive pancreatic adenocarcinomas (15 of 20); no TP53 mutations were found in PanIN-1 lesions or low-grade IPMNs.]. 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:23200980; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP924970.RAigVnx85F128dJzW9hV5qlzICgo77c64gVaP6Ot7agkI130_publicationInfo { this: dcterms:created "2015-08-25T14:47:04+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }