Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_assertion description "[Niemann-Pick type C (NPC) disease is an autosomal recessive disorder caused by mutations of NPC1 and NPC2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_assertion evidence source_evidence_literature NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_assertion SIO_000772 17631520 NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_assertion wasDerivedFrom befree-20140225 NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_assertion wasGeneratedBy ECO_0000203 NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_provenance.