Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_assertion wasGeneratedBy ECO_0000203 NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_assertion wasDerivedFrom befree-2016 NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_assertion SIO_000772 12215093 NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_assertion evidence source_evidence_literature NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.
- NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_assertion description "[Patients with POAG who harbored the rarer allele of the MYOC.mt1 promoter polymorphism were no different from those with the more common variant in any measure of disease severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367062.RA7yvScdKI4yIQ-D9gwjva49Ubk3tAkmBK0XDPsG3ewlQ130_provenance.