Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_assertion> ?p ?o ?g. }
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- NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_assertion type Assertion NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_head.
- NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_assertion description "[It has recently been demonstrated that genetic defects in keratin genes cause a number of different skin disorders, including epidermolysis bullosa simplex (EBS), epidermolytic hyperkeratosis (EH), the EH form of epidermal nevi, epidermolytic and non-epidermolytic forms of palmoplantar keratoderma (EPPK and PPK) and pachyonychia congenita (PC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_provenance.
- NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_assertion evidence source_evidence_literature NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_provenance.
- NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_assertion SIO_000772 9023700 NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_provenance.
- NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_assertion wasDerivedFrom befree-20150227 NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_provenance.
- NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_assertion wasGeneratedBy ECO_0000203 NP528924.RA3UfDzQ2Er5jL1YRNROt3lSStZNvlojDTV4I4raDdBuY130_provenance.