Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_assertion description "[Similarly, no statistically significant difference was found in IL1RN and IL1B (-511 and +3953) allele frequencies between CAD and control subjects, MVD and control subjects or SVD and control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_assertion evidence source_evidence_literature NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_assertion SIO_000772 19142372 NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_assertion wasDerivedFrom befree-20140225 NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_assertion wasGeneratedBy ECO_0000203 NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP502114.RAmHbcg8Fm5_lLl1F2B_vbs1XbJoYQEhDBx_s8ic-Is9s130_provenance.