Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_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." NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_assertion evidence source_evidence_literature NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_assertion SIO_000772 10430828 NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_assertion wasDerivedFrom befree-20140225 NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_assertion wasGeneratedBy ECO_0000203 NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP439163.RAK6H_gukbs4Kdb0IQKviZXg3saGnRHJHskWl49VKwK2w130_provenance.