Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_assertion evidence source_evidence_literature NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_assertion SIO_000772 16333318 NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_assertion wasDerivedFrom gad-20150221 NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_assertion wasGeneratedBy ECO_0000203 NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.