Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_assertion description "[These advances have combined the approaches of positional cloning and candidate gene analysis to great effect, with the pivotal role of the dystrophin-associated complex confirmed through the involvement of at least four dystrophin-associated proteins in different subtypes of autosomal recessive LGMD (the sarcoglycanopathies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_assertion evidence source_evidence_literature NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_assertion SIO_000772 10430828 NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_assertion wasDerivedFrom befree-2016 NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_assertion wasGeneratedBy ECO_0000203 NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.
- befree-2016 importedOn "2016-02-19" NP259182.RA0QybXy0R8_W2mcWKhIodaCsOrrLddJAdD1Fff4KRzko130_provenance.