Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_assertion> ?p ?o ?g. }
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- NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_assertion type Assertion NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_head.
- NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_assertion description "[Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disease caused by mutations in the cytochrome P450(27) (CYP27) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_provenance.
- NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_assertion evidence source_evidence_literature NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_provenance.
- NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_assertion SIO_000772 8728324 NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_provenance.
- NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_assertion wasDerivedFrom befree-20150227 NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_provenance.
- NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_assertion wasGeneratedBy ECO_0000203 NP345677.RAC4wT1U0q7C1Z2R0M13dT3T_2dZRMzTB6dsfUEfvvLQY130_provenance.