Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_assertion description "[We searched for mutations in the KRT5 gene, a causative gene for the similar pigmentation disorder Dowling-Degos disease (DDD), in all the patients and found no KRT5 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_assertion evidence source_evidence_literature NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_assertion SIO_000772 23666529 NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_assertion wasDerivedFrom befree-20140225 NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_assertion wasGeneratedBy ECO_0000203 NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP683837.RAeZYMBoTqzIku9FPrh3cBzllNDAftNT3cJFfqHHEVpCY130_provenance.