Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_assertion description "[The common variant in the human complement Factor H gene (CFH), with Tyr402His, is linked to age-related macular degeneration (AMD), a prevalent disorder leading to visual impairment and irreversible blindness in elderly patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_assertion evidence source_evidence_literature NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_assertion SIO_000772 17399790 NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_assertion wasDerivedFrom befree-20140225 NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_assertion wasGeneratedBy ECO_0000203 NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP721892.RAwBnrAzle3OSMYJpmqvpSpcdarguAou4NvObHaqY0X5Q130_provenance.