Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_assertion> ?p ?o ?g. }
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- NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_assertion type Assertion NP239055.RAW0FpJCI5JV-Jc8qZy_QkB85Zv2sOSciNSsUurFxpe4A130_head.
- 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.