Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_assertion> ?p ?o ?g. }
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- NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_assertion type Assertion NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_head.
- NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_assertion description "[Although deletion of STS in males is known to cause X-linked ichthyosis, the clinical significance of STS copy gains is less clear, with the duplication reported in individuals with abnormal phenotypes and normal relatives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_provenance.
- NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_assertion evidence source_evidence_literature NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_provenance.
- NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_assertion SIO_000772 21739574 NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_provenance.
- NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_assertion wasDerivedFrom befree-2016 NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_provenance.
- NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_assertion wasGeneratedBy ECO_0000203 NP908131.RACAozZvZvta7aSKYiizlkBcCraiNEBwSm0xxXLjI1I7s130_provenance.