Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_assertion description "[Support, including replication evidence, was obtained for nine T1D associated variants in genes ITGB7 (rs11170466, P=7.86�10-9), NRP1 (rs722988, 4.88�10-8), BAD (rs694739, 2.37�10-7), CTSB (rs1296023, 2.79�10-7), FYN (rs11964650, P=5.60�10-7), UBE2G1 (rs9906760, 5.08�10-7), MAP3K14 (rs17759555, 9.67�10-7), ITGB1 (rs1557150, 1.93�10-6), and IL7R (rs1445898, 2.76�10-6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_assertion evidence source_evidence_literature NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_assertion SIO_000772 25371288 NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_assertion wasDerivedFrom befree-2016 NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_assertion wasGeneratedBy ECO_0000203 NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1235156.RA046qxKyaADyvEN45LYutlJdEhzLe1mr1eLE2IebUR4w130_provenance.