Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_assertion description "[We initially conducted a comparative genetic analysis of neovascular AMD and PCV, genotyping the ARMS2 A69S variant in 181 subjects with neovascular AMD, 198 subjects with PCV, and 203 controls in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_assertion evidence source_evidence_literature NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_assertion SIO_000772 22219653 NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_assertion wasDerivedFrom befree-20140225 NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_assertion wasGeneratedBy ECO_0000203 NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505006.RA0Vlzol37jFtDMurm7izUbklegjT4-gWZwfkNEPwxDB4130_provenance.