Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_assertion wasGeneratedBy ECO_0000218 NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_assertion wasDerivedFrom ctd_human-20150221 NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_assertion SIO_000772 17376794 NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_assertion evidence source_evidence_curated NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_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." NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.