Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion description "[To date, all identified causative mutations for CS have been in the two known CS-associated genes, ERCC8 (CSA) and ERCC6 (CSB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion evidence source_evidence_literature NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion SIO_000772 23623389 NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion wasDerivedFrom befree-20150227 NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion wasGeneratedBy ECO_0000203 NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.