Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_assertion description "[Within this region, we defined a 42-SNP haplotype that was associated with significantly increased risk of ALS (p=7�47�10(-33) when people with familial ALS were compared with controls, odds ratio 21�0, 95% CI 11�2-39�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." NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_assertion evidence source_evidence_literature NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_assertion SIO_000772 20801718 NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_assertion wasDerivedFrom befree-20140225 NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_assertion wasGeneratedBy ECO_0000203 NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP242205.RAQJ3TkYsTpGSRz-IIgDeRzU7xmMIFmagPaiT1CoCy6MY130_provenance.