Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_assertion description "[Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_assertion evidence source_evidence_literature NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_assertion SIO_000772 15610558 NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_assertion wasDerivedFrom gad-20150221 NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_assertion wasGeneratedBy ECO_0000203 NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP89636.RArUenXIRr6iVcfJbtqNqVE2bgfX9JQWDVCO7xLCLkMVw130_provenance.