Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_assertion description "[Homozygosity at the HLA-DQA1 locus was found to be a genetic risk factor unique to familial IIM (57% versus 24% of controls; odds ratio 4.2, corrected P = 0.002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_assertion evidence source_evidence_literature NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_assertion SIO_000772 9550481 NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_assertion wasDerivedFrom befree-2016 NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_assertion wasGeneratedBy ECO_0000203 NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1393350.RAiWbRvEIGZxv2T-H5tUtoLzGt3yzhzedLjP1YLXR9Nq4130_provenance.