Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_assertion description "[A novel mutation in AlphaA-crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_assertion evidence source_evidence_literature NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_assertion SIO_000772 18407550 NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_assertion wasDerivedFrom befree-20140225 NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_assertion wasGeneratedBy ECO_0000203 NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.
- befree-20140225 importedOn "2014-02-25" NP489879.RApUaThkShINBxcaCnmX6xL4nVWRtR7-f25YepcTiH_us130_provenance.