@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:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_head { this: np:hasAssertion dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_assertion; np:hasProvenance dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_provenance; np:hasPublicationInfo dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_publicationInfo; a np:Nanopublication . dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_assertion a np:Assertion . dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_provenance a np:Provenance . dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_publicationInfo a np:PublicationInfo . } dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_assertion { miriam-gene:2697 a ncit:C16612 . lld:C0004114 a ncit:C7057 . dgn-gda:DGNdc84a3f6b43f9e08ffa55bf995d24618 sio:SIO_000628 miriam-gene:2697, lld:C0004114; a sio:SIO_001121 . } dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_provenance { dgn-np:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_assertion dcterms:description "[To gain access to the role played by gap junctional communication in ICW propagation generated by P2YR activation, we selectively expressed P2Y(1,2,4)R subtypes and Cx43 in the human 1321N1 astrocytoma cell line, which lacks endogenous P2 receptors.]. 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:15390120; 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:NP425369.RAJZcKNip50TI2qREsXtEJUUn4-2l26ZYZlQL6Iom7zbw130_publicationInfo { this: dcterms:created "2015-08-25T14:41:47+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" . }