Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_assertion> ?p ?o ?g. }
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- NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_assertion type Assertion NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_head.
- NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_assertion wasGeneratedBy ECO_0000203 NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_provenance.
- NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_assertion wasDerivedFrom befree-2016 NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_provenance.
- NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_assertion SIO_000772 20523032 NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_provenance.
- NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_assertion evidence source_evidence_literature NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_provenance.
- NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_assertion description "[X-linked ichthyosis (XLI) is a relatively common keratinization disorder which is caused, in the vast majority of cases, by a total deletion of the sulfatase steroid (STS) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816508.RAyM3xnmewwPFSWMiEr4Kj3GKua4KRV3ecMaFnSqWweLg130_provenance.