Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion description "[The conflicting evidence on disease association and the lack of association between disease and particular populations, despite the wide range of HP(1) and HP(2) gene frequencies across the world, may indicate that any associations are marginal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion evidence source_evidence_literature NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion SIO_000772 17474882 NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion wasDerivedFrom befree-20140225 NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion wasGeneratedBy ECO_0000203 NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance.