Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_assertion> ?p ?o ?g. }
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- NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_assertion type Assertion NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_head.
- NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_assertion description "[Cerebrotendinous Xanthomatosis (CTX) is a rare autosomal recessive lipid storage disease caused by sterol 27-hydroxylase (CYP27) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_provenance.
- NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_assertion evidence source_evidence_literature NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_provenance.
- NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_assertion SIO_000772 21958693 NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_provenance.
- NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_assertion wasDerivedFrom befree-20140225 NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_provenance.
- NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_assertion wasGeneratedBy ECO_0000203 NP490025.RA-kiSP5ZnBdYdRVhkkL0EAv6ku3tPkLgUfvQWS66tswU130_provenance.