Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_assertion description "[According to SNP genotyping in 73 subjects, there was no significant difference of IOP between subjects with different CYP2D6 Arg296Cys (P = 0.308) or Ser486Thr genotypes (P = 0.741).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_assertion evidence source_evidence_literature NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_assertion SIO_000772 19284319 NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_assertion wasDerivedFrom befree-20140225 NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_assertion wasGeneratedBy ECO_0000203 NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP252837.RAPggxPSXZynOsgsTnxbGr3ZSmBFGk1sL3Z7r3iM94arg130_provenance.