Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_assertion description "[In order to investigate the role of variation in NLR genes for AD, we genotyped 23 single nucleotide polymorphisms (SNPs) in seven selected NLR genes (CARD4, CARD15, CARD12, NALP1, NALP3, NALP12, MHC2TA) in 392 AD patients and 297 controls by restriction enzyme digestion or TaqMan assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_assertion evidence source_evidence_literature NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_assertion SIO_000772 17620097 NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_assertion wasDerivedFrom befree-20150227 NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_assertion wasGeneratedBy ECO_0000203 NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP842233.RAwmiBGmRCU3Nv_DkhYyG8Xbpk3ORV2OGy9SrmQK4RIX8130_provenance.