Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_assertion description "[In their model, SMaRT was able to replace a mutation of the plectin gene in epidermolysis bullosa simplex with muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_assertion evidence source_evidence_literature NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_assertion SIO_000772 18268535 NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_assertion wasDerivedFrom befree-2016 NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_assertion wasGeneratedBy ECO_0000203 NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.
- befree-2016 importedOn "2016-02-19" NP655033.RATy161H4sUXAkxHNGWRAfAExrwYIhPJYf9xnSZPfUmuI130_provenance.