Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_assertion description "[A novel (967-970+2)delAAAGGT mutation existed in the CHM gene of a Japanese family with choroideremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_assertion evidence source_evidence_literature NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_assertion SIO_000772 18773267 NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_assertion wasDerivedFrom befree-2016 NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_assertion wasGeneratedBy ECO_0000203 NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.
- befree-2016 importedOn "2016-02-19" NP691654.RAYj9HbQaWYeToh0IQlE36YMRm9WXUnC4QLHdFZ-eOi3E130_provenance.