@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:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_head { this: np:hasAssertion dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_assertion; np:hasProvenance dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_provenance; np:hasPublicationInfo dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_publicationInfo; a np:Nanopublication . dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_assertion a np:Assertion . dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_provenance a np:Provenance . dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_publicationInfo a np:PublicationInfo . } dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_assertion { miriam-gene:3845 a ncit:C16612 . lld:C0027627 a ncit:C7057 . dgn-gda:DGN2c40129dd5ac00e2e820055884e62e2b sio:SIO_000628 miriam-gene:3845, lld:C0027627; a sio:SIO_001121 . } dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_provenance { dgn-np:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_assertion dcterms:description "[The c-K-ras 2 codon 12 mutation frequency was 0/30 in normal tissues, 0/17 in adenomas with mild atypia, 3/37 (8.1%) in adenomas with moderate atypia, 15/18 (83.3%) in adenomas with severe atypia, 19/73 (26.0%) in primary carcinomas and 3/13 (23.1%) in metastatic tumors.]. 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:1708754; 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:NP577971.RAEQscYsvFdxj1A7St3we3NsKB4_YRoHKIqCTBwUjXdxU130_publicationInfo { this: dcterms:created "2016-05-13T12:46:07+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" . }