@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:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_head { this: np:hasAssertion dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_assertion; np:hasProvenance dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_provenance; np:hasPublicationInfo dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_publicationInfo; a np:Nanopublication . dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_assertion a np:Assertion . dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_provenance a np:Provenance . dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_publicationInfo a np:PublicationInfo . } dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_assertion { miriam-gene:7422 a ncit:C16612 . lld:C0027627 a ncit:C7057 . dgn-gda:DGNe68f3124e87b15ab84e642a07819d550 sio:SIO_000628 miriam-gene:7422, lld:C0027627; a sio:SIO_001121 . } dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_provenance { dgn-np:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_assertion dcterms:description "[A number of invasion and metastasis predictive genes (including plasminogen activator; matrix metalloproteinase; matrix structural constituent genes encoding products with collagen, heparin, and hyaluronic acid binding activity; genes encoding receptors for insulin-like growth factors; vascular endothelial growth factor; endothelin type A; fibroblast growth factor; thrombospondin 1 and 2; type A and B integrins, and chemokines [stromal cell-derived factor 1 (CXCL12)]) were found among the 120 genes that were highly differentially overexpressed in MET, when compared with OSPC.]. 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:17346539; 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:NP597881.RA3L-Gg3l4amKT0ZvBKoCc0vIn2ceXHLJjA0gF_oL6n1g130_publicationInfo { this: dcterms:created "2016-05-13T12:46:16+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" . }