Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_assertion description "[As expected, all CD patients had at least one of the CD-associated alleles, and the highest CD risk was indicated by the presence of the HLA-DQ2.5 heterodimer (HLA-DQA1*05-DQB1*02) with HLA-DQB1*02 in homozygosity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_assertion evidence source_evidence_literature NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_assertion SIO_000772 25413104 NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_assertion wasDerivedFrom befree-2016 NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_assertion wasGeneratedBy ECO_0000203 NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238958.RA-nU0Qa3lt7zf5Pgiz3TQZlEgyoODsCujernDPf09I1U130_provenance.