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- NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_assertion type Assertion NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_head.
- NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_assertion description "[Niemann-Pick type C1 disease (NPC1) is an autosomal recessive neurovisceral storage disease caused by the mutation of NPC1 gene, resulting in perturbed intracellular transport of unesterified cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_provenance.
- NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_assertion evidence source_evidence_literature NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_provenance.
- NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_assertion SIO_000772 15099022 NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_provenance.
- NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_assertion wasDerivedFrom befree-20150227 NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_provenance.
- NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_assertion wasGeneratedBy ECO_0000203 NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_provenance.