Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_assertion description "[TLR4 variant genotype was more common in CD patients without MBL deficiency (11% vs. 1.7%, OR: 7.29, 95% CI: 1.08-53.9, p = 0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_assertion evidence source_evidence_literature NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_assertion SIO_000772 20079790 NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_assertion wasDerivedFrom befree-20140225 NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_assertion wasGeneratedBy ECO_0000203 NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP915020.RAOzZXc4Ezz2TZvTaPNHlAp5ljDFMWMDdiEmzcw7SmjZI130_provenance.