Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_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." NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_assertion evidence source_evidence_literature NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_assertion SIO_000772 17620097 NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_assertion wasDerivedFrom befree-2016 NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_assertion wasGeneratedBy ECO_0000203 NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.
- befree-2016 importedOn "2016-02-19" NP619205.RA7JpTt1NHBIJPrdOCEGT_FZuuNMiwgW_VluZu4nIEmb8130_provenance.