Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_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." NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_assertion evidence source_evidence_literature NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_assertion SIO_000772 1642226 NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_assertion wasDerivedFrom befree-20150227 NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_assertion wasGeneratedBy ECO_0000203 NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP319191.RAoxeO1E6Gp7d4IBLz0gYa9_9gE928Tz0zKsHkYua27PM130_provenance.