Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_assertion description "[We report here that two variants in the organic cation transporter cluster at 5q31 (a missense substitution in SLC22A4 and a G-->C transversion in the SLC22A5 promoter) form a haplotype associated with susceptibility to Crohn disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_assertion evidence source_evidence_literature NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_assertion SIO_000772 15107849 NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_assertion wasDerivedFrom gad-20130706 NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_assertion wasGeneratedBy ECO_0000203 NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.