Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_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." NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_assertion evidence source_evidence_literature NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_assertion SIO_000772 17383044 NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_assertion wasDerivedFrom befree-2016 NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_assertion wasGeneratedBy ECO_0000203 NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.
- befree-2016 importedOn "2016-02-19" NP600742.RAraTtmr1Go3Gx_Bk5jxSU0EE3GOOeNAXnDNTt76oyfd8130_provenance.