Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_assertion description "[Here, we tested the hypothesis that PRNP is a disease-modifying gene in clinical Wilson disease with a neurological phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_assertion evidence source_evidence_literature NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_assertion SIO_000772 16543824 NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_assertion wasDerivedFrom befree-20140225 NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_assertion wasGeneratedBy ECO_0000203 NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP604356.RAhbKa7b7359nFflb8Pxr9N8AXD4N1K9iiENRI9SDW7O8130_provenance.