Matches in Nanopublications for { ?s ?p "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP694396.RAv8rOTihESJEYfhTflsPA9y_guDXlTH7QOWA70mDD-bs130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694396.RAv8rOTihESJEYfhTflsPA9y_guDXlTH7QOWA70mDD-bs130_provenance.
- NP492399.RAT1QcyhEMR4TRQ1BLNU9Ty5PoSfXymgQlPNEY9nO8B5U130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492399.RAT1QcyhEMR4TRQ1BLNU9Ty5PoSfXymgQlPNEY9nO8B5U130_provenance.
- NP31268.RA5uEYOoT1DgscTLyAAUK66BZlz8NEZN4N68iEl6w2YBI130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31268.RA5uEYOoT1DgscTLyAAUK66BZlz8NEZN4N68iEl6w2YBI130_provenance.
- NP547998.RAL42lEiSXqB0d_kK7WWB00XIJWkl1HniACfe3qR6lg0g130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547998.RAL42lEiSXqB0d_kK7WWB00XIJWkl1HniACfe3qR6lg0g130_provenance.
- assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP715174.RAuCPMyVi8vKCebpFukSvAV6AFv6qknVALTu-DcZ3t5D8130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715174.RAuCPMyVi8vKCebpFukSvAV6AFv6qknVALTu-DcZ3t5D8130_provenance.
- NP715266.RAuKcSj6D57QPKNAoF_4EtKzW1PaoMU8Yi3N0xQGQsUEU130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715266.RAuKcSj6D57QPKNAoF_4EtKzW1PaoMU8Yi3N0xQGQsUEU130_provenance.
- NP668460.RAUCuNc5AGodyv4npA-LI5VTOM9E37KOsGHV3JKqcZZjw130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668460.RAUCuNc5AGodyv4npA-LI5VTOM9E37KOsGHV3JKqcZZjw130_provenance.
- NP668459.RArGNNkiDOXkZ8q74KktXETxqh0ZxTnlswGc4vmtJej48130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668459.RArGNNkiDOXkZ8q74KktXETxqh0ZxTnlswGc4vmtJej48130_provenance.
- NP715199.RAMHkJNid_5Wy_G-2NYOzQJsjDQaN_TqIvQml08rv-0G4130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715199.RAMHkJNid_5Wy_G-2NYOzQJsjDQaN_TqIvQml08rv-0G4130_provenance.
- NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_provenance.