Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion> ?p ?o ?g. }
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- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion type Assertion NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_head.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion wasGeneratedBy ECO_0000203 NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion wasDerivedFrom befree-2016 NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion SIO_000772 24848304 NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion evidence source_evidence_literature NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion description "[Netherton syndrome (NS; OMIM 256500) is a genetic skin disease resulting from defects in the serine protease inhibitor Kazal-type 5 (SPINK5) gene, which encodes the protease inhibitor lympho-epithelial Kazal type inhibitor (LEKTI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.