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- source_evidence_literature type ECO_0000212 NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_assertion description "[Mutations in the human RDS gene are responsible for several forms of inherited blindness including autosomal-dominant retinitis pigmentosa and macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_assertion evidence source_evidence_literature NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_assertion SIO_000772 10704489 NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_assertion wasDerivedFrom befree-20150227 NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_assertion wasGeneratedBy ECO_0000203 NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760999.RAPhlZmjHoiOO8624gLNXQzkoTQf6ehYZw1zcSrlngeJs130_provenance.