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- NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_assertion type Assertion NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_head.
- NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_assertion wasGeneratedBy ECO_0000203 NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_provenance.
- NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_assertion wasDerivedFrom befree-20150227 NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_provenance.
- NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_assertion SIO_000772 17003072 NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_provenance.
- NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_assertion evidence source_evidence_literature NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_provenance.
- NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_assertion description "[Niemann-Pick disease type C (NPC) is a fatal neurovisceral lipid storage disease of autosomal inheritance resulting from mutations in either the NPC1 (95% of families) or NPC2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982215.RAlBTkxpXbYWct8fqZjMnh55iSX-5-qR6w2ApsDleeAuM130_provenance.