Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_assertion evidence source_evidence_literature NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_assertion SIO_000772 17376794 NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_assertion wasDerivedFrom befree-20150227 NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_assertion wasGeneratedBy ECO_0000203 NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.