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- source_evidence_literature type ECO_0000212 NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_assertion description "[Within this region, we defined a 42-SNP haplotype that was associated with significantly increased risk of ALS (p=7A*47A10(-33) when people with familial ALS were compared with controls, odds ratio 21A*0, 95% CI 11A*2-39A*1) and which overlapped with an association locus recently reported for frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_assertion evidence source_evidence_literature NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_assertion SIO_000772 20801718 NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_assertion wasDerivedFrom gad-20150221 NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_assertion wasGeneratedBy ECO_0000203 NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.
- gad-20150221 importedOn "2015-02-21" NP63636.RAED3OOuKlf9o81LibGaa613qh_sFzrUXHzLLSff-NJ5w130_provenance.