Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_assertion description "[We investigated 29 single nucleotide polymorphisms (SNPs) within the P2RX7 gene and adjacent genes in a sample of 1000 German Caucasian patients suffering from recurrent major depressive disorder (MDD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_assertion evidence source_evidence_literature NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_assertion SIO_000772 16822851 NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_assertion wasDerivedFrom gad-20130706 NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_assertion wasGeneratedBy ECO_0000203 NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130_provenance.