Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_assertion description "[This polymorphism results in an amino acid exchange in the C-terminal cytosolic domain of the P2RX7 channel protein, suggesting that the observed P2RX7 polymorphism might play a causal role in the development of depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_assertion evidence source_evidence_literature NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_assertion SIO_000772 16822851 NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_assertion wasDerivedFrom befree-20140225 NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_assertion wasGeneratedBy ECO_0000203 NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP587036.RAZWICfbTKE50UQFHxPNa0MFMts9fcmzUUUInbREVGy7I130_provenance.