Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_assertion description "[Dominantly inherited cataracts with differing clinical features were found in two families carrying different point mutations in the gene encoding lens water channel protein AQP0 (major intrinsic protein, MIP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_assertion evidence source_evidence_literature NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_assertion SIO_000772 11001937 NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_assertion wasDerivedFrom befree-20140225 NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_assertion wasGeneratedBy ECO_0000203 NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP646387.RArME0zUsK9U312_LFdWITNZyb9dLHv2nRvLGSKIeFp-M130_provenance.