Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_assertion description "[Single-SNP analysis demonstrated significant associations of the CARD15_R702W variation and the NALP12_In9 T-allele with AD (P = 0.008 and P = 0.03, resp.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_assertion evidence source_evidence_literature NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_assertion SIO_000772 17620097 NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_assertion wasDerivedFrom befree-20150227 NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_assertion wasGeneratedBy ECO_0000203 NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960855.RA0ZyWtI51xw4kSagMGN1a3-acuFzgl5OvDN5n2KzsMIo130_provenance.