Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_assertion description "[we observe significant association with risk for AD and polymorphisms in ACE, CHRNB2, TF, and an as yet uncharacterized locus on chromosome 7p15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_assertion evidence source_evidence_literature NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_assertion SIO_000772 18830724 NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_assertion wasDerivedFrom gad-20130706 NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_assertion wasGeneratedBy ECO_0000203 NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.
- gad-20130706 importedOn "2013-07-06" NP50751.RA5vxKz_sEt1pLUK7wjw5WT349zdlEdnYY8dTlVil9Fa4130_provenance.