Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP1184349.RAUZDVth4t1eGLEgk7u51OekuvjyB6U4qsEYnjE8H4HUI130_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." NP1184349.RAUZDVth4t1eGLEgk7u51OekuvjyB6U4qsEYnjE8H4HUI130_provenance.
- 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." provenance.
- 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." provenance.
- 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." 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.
- NP1184351.RAtqlN4328Cq3zAQp6mA5jVzCzz8u01DRaAM6YtcTpTzI130_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." NP1184351.RAtqlN4328Cq3zAQp6mA5jVzCzz8u01DRaAM6YtcTpTzI130_provenance.