Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_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." NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_assertion evidence source_evidence_literature NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_assertion SIO_000772 17383044 NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_assertion wasDerivedFrom befree-20140225 NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_assertion wasGeneratedBy ECO_0000203 NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP773942.RAy9I13-t9fnh_i_cCboSN8ssUTiBbUkUeYwAFvb8Qd8I130_provenance.