@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:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_head { this: np:hasAssertion dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_assertion; np:hasProvenance dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_provenance; np:hasPublicationInfo dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_publicationInfo; a np:Nanopublication . dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_assertion a np:Assertion . dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_provenance a np:Provenance . dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_publicationInfo a np:PublicationInfo . } dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_assertion { miriam-gene:1796 a ncit:C16612 . lld:C0699791 a ncit:C7057 . dgn-gda:DGN4be8957b4f7ad6a1d7605e26afaaa47b sio:SIO_000628 miriam-gene:1796, lld:C0699791; a sio:SIO_001121 . } dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_provenance { dgn-np:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_assertion dcterms:description "[Among differentially methylated genes, we identified new genes (CHRNA3 and DOK1) as targets of aberrant hypermethylation in GC, suggesting that epigenetic deregulation of these genes and their corresponding cellular pathways may promote the development and progression of GC.]. 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:21831520; 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:NP916098.RAJQN5uoGze_wZlH1nhzfR3Hw-zFI8iF0XswZy15wR-vc130_publicationInfo { this: dcterms:created "2016-05-13T12:48:39+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }