Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_assertion description "[Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_assertion evidence source_evidence_literature NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_assertion SIO_000772 16036915 NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_assertion wasDerivedFrom befree-20140225 NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_assertion wasGeneratedBy ECO_0000203 NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453681.RAOa3kVH7PDq1pV_o00b7jqgOqFbGoHpsD2JyW5ZsVcCY130_provenance.