Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_assertion> ?p ?o ?g. }
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- NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_assertion type Assertion NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_head.
- NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_assertion wasGeneratedBy ECO_0000203 NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_provenance.
- NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_assertion wasDerivedFrom befree-20140225 NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_provenance.
- NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_assertion SIO_000772 10597140 NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_provenance.
- NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_assertion evidence source_evidence_literature NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_provenance.
- NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_assertion description "[Epidermolytic hyperkeratosis (EHK) is a genodermatosis caused by mutations in either the keratin 1 (K1) or keratin 10 (K10) genes, and characterized by erythroderma and blistering at birth, with development of a ribbed, ichthyotic hyperkeratosis and palmoplantar keratoderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627955.RAHGYl4FCyJ6fYDgEtCG-a9c5clEwnOr32_W0F5wPEivg130_provenance.