Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_assertion description "[The population attributable fraction (PAF) due to the ADH1B*2 allele was 29% for LC, 47% for CP, and 27% for DM, and the PAF due to the ALDH2*1/*1 genotype was 26% for LC, 34% for DM, and 30% for HT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_assertion evidence source_evidence_literature NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_assertion SIO_000772 23550892 NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_assertion wasDerivedFrom befree-20140225 NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_assertion wasGeneratedBy ECO_0000203 NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP796823.RAwv6tbd9eL48RBknfqlJtPDRiGoXqMJ_n3-MD_UslgOE130_provenance.