Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_assertion> ?p ?o ?g. }
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- NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_assertion type Assertion NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_head.
- NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_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." NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_provenance.
- NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_assertion evidence source_evidence_literature NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_provenance.
- NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_assertion SIO_000772 1642226 NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_provenance.
- NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_assertion wasDerivedFrom befree-20150227 NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_provenance.
- NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_assertion wasGeneratedBy ECO_0000203 NP319361.RATD-IXeF_btyu1ClC6fOo6um1UsdzhcQPyBPqUzy3N0Q130_provenance.