Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_assertion type Assertion NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_head.
- NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_assertion wasGeneratedBy ECO_0000203 NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_provenance.
- NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_assertion wasDerivedFrom befree-2016 NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_provenance.
- NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_assertion SIO_000772 10408773 NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_provenance.
- NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_assertion evidence source_evidence_literature NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_provenance.
- NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_assertion description "[The Hallopeau-Siemens variant of recessive dystrophic epidermolysis bullosa (HS-RDEB) is a severe inherited skin disease characterized by the absence of collagen type VII (COLVII) and anchoring fibrils (AF), caused by mutations in collagen type VII gene (COL7A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257920.RAtmbjWF1iW2FuC8CegdHB9WpA8bjln1LqCngOnG0Va60130_provenance.