Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_assertion description "[The identification of TREX1 mutations in families with retinal vasculopathy and associated diseases such as migraine may provide new insights in migraine pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_assertion evidence source_evidence_literature NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_assertion SIO_000772 18451712 NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_assertion wasDerivedFrom befree-20150227 NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_assertion wasGeneratedBy ECO_0000203 NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP863875.RAHv2EzuNU4Bii6dtkerkm3y5SD9AbTPGGECFpYtyopTE130_provenance.