Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_assertion description "[We observed that, in combination, allelic variants in the COX2, IL18, ILR4, and IL10 genes modify the risk for developing HD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_assertion evidence source_evidence_literature NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_assertion SIO_000772 21061265 NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_assertion wasDerivedFrom befree-20140225 NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_assertion wasGeneratedBy ECO_0000203 NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP865146.RAnY5wo_Vk1hRt3keJxOXggHipJVGd-SbU3vzw3bBWZLo130_provenance.