Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_assertion description "[identified ACVRL1 mutations in hereditary hemorrhagic telangiectasia, including 4 unknown, and found that ACVRL1, and not ENG, mutations are predictive for liver disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_assertion evidence source_evidence_literature NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_assertion SIO_000772 18498373 NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_assertion wasDerivedFrom lhgdn-20090331 NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_assertion wasGeneratedBy ECO_0000203 NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP238067.RAuxHKOl53YC7cb__73RNF8JCw24e6t3CB5gsVX4pv4WA130_provenance.