Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_assertion description "[Also, the D-del-I haplotype was associated with a significantly lower CM risk (OR, 0.52; 95% CI, 0.37-0.74; FPRP, 0.04) than was the most common haplotype, D-ins-I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_assertion evidence source_evidence_literature NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_assertion SIO_000772 18563783 NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_assertion wasDerivedFrom befree-20140225 NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_assertion wasGeneratedBy ECO_0000203 NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297884.RAZ2jat8AOZ10dPLdeqj5YEYmuDm8gVPXeTdrZ8VTOegk130_provenance.