Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_assertion> ?p ?o ?g. }
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- NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_assertion type Assertion NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_head.
- NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_assertion wasGeneratedBy ECO_0000203 NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_provenance.
- NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_assertion wasDerivedFrom befree-20140225 NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_provenance.
- NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_assertion SIO_000772 21544567 NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_provenance.
- NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_assertion evidence source_evidence_literature NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_provenance.
- NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_assertion description "[While CGI-58 mutations are associated with Chanarin-Dorfman syndrome, a condition characterized by lipid storage and skin involvement (ichthyosis), mutations in the patatin-like phospholipase domain-containing protein 2 gene (PNPLA2) were reported with skeletal and cardiac muscle disease only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707387.RALUGVm4Qodmmk98wljxzaQkFcHJ2_TLn5LpqaSzK9UCA130_provenance.