Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_assertion description "[Two HLA risk haplotypes in PSC (carrying DRB1*0301 or DRB1*1501, respectively) were devoid of both of these alleles, and carried the 5.1 variant of the major histocompatibility complex class I chain-related A (MICA) gene previously reported to influence PSC susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_assertion evidence source_evidence_literature NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_assertion SIO_000772 17383044 NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_assertion wasDerivedFrom gad-20150221 NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_assertion wasGeneratedBy ECO_0000203 NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP106333.RAtglabq37FxH2kT2j8pmjhjpXk2saV2ShWV0OiQeWGE0130_provenance.