Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_assertion> ?p ?o ?g. }
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- NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_assertion type Assertion NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_head.
- NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_assertion description "[Dermatosparaxis is a recessively inherited connective-tissue disorder that results from lack of the activity of type I procollagen N-proteinase, the enzyme that removes the amino-terminal propeptides from type I procollagen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_provenance.
- NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_assertion evidence source_evidence_literature NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_provenance.
- NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_assertion SIO_000772 1642226 NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_provenance.
- NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_assertion wasDerivedFrom befree-20140225 NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_provenance.
- NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_assertion wasGeneratedBy ECO_0000203 NP682398.RA6M5NUltksczKyIZX4W1aX_SlGJBJRzhuGglUQaYc1fk130_provenance.