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- source_evidence_literature type ECO_0000212 NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_assertion description "[In fact, a recent study identified a functional single nucleotide polymorphism (SNP) within the first common exon of CHAT, which was associated with AD giving an odds ratio of 3.8 (Neurosci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_assertion evidence source_evidence_literature NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_assertion SIO_000772 12770689 NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_assertion wasDerivedFrom befree-20140225 NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_assertion wasGeneratedBy ECO_0000203 NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717674.RA2ALEXEEzn30lwFPcbjhvMCs8NOm_6KaNk4gpBNio0mc130_provenance.