@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:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_head { this: np:hasAssertion dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_assertion; np:hasProvenance dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_provenance; np:hasPublicationInfo dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_publicationInfo; a np:Nanopublication . dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_assertion a np:Assertion . dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_provenance a np:Provenance . dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_publicationInfo a np:PublicationInfo . } dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_assertion { miriam-gene:4921 a ncit:C16612 . lld:C0007137 a ncit:C7057 . dgn-gda:DGNd8cf8d3c03cfd71387af80753e055927 sio:SIO_000628 miriam-gene:4921, lld:C0007137; a sio:SIO_001122 . } dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_provenance { dgn-np:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_assertion dcterms:description "[These data indicated that the novel DDR2 mutation may contribute to the development and progression of lung SCC and this effect may be associated with increased proliferation and invasiveness, at least in part, via regulating E-cadherin expression.]. 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:24885564; 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:NP600564.RAeeeylQIEBbHxH_l7p1nETQ5tOEamMD3O3oMyy6wfMyk130_publicationInfo { this: dcterms:created "2015-08-25T14:43:39+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" . }