Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_assertion description "[Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_assertion evidence source_evidence_literature NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_assertion SIO_000772 14583443 NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_assertion wasDerivedFrom gad-20130706 NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_assertion wasGeneratedBy ECO_0000203 NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP46895.RAfK4NluiZHM2QtUiujjksighsOmg7eJbwEYlvhzPGAlw130_provenance.