Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_assertion evidence source_evidence_literature NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_assertion SIO_000772 12840783 NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_assertion wasDerivedFrom befree-20140225 NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_assertion wasGeneratedBy ECO_0000203 NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.