Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_assertion description "[Heterozygous mutations in ELOVL4, the gene encoding one of the elongases, are known to cause macular degeneration in humans and retinal abnormalities in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_assertion evidence source_evidence_literature NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_assertion SIO_000772 22100072 NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_assertion wasDerivedFrom befree-20140225 NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_assertion wasGeneratedBy ECO_0000203 NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP354013.RAYZjEzD6rMpS0Etfck3Guh6QL4B5bhin_09RHVkmvL6Q130_provenance.