Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_assertion wasGeneratedBy ECO_0000203 NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_assertion wasDerivedFrom befree-20150227 NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_assertion SIO_000772 22468107 NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_assertion evidence source_evidence_literature NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.
- NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_assertion description "[The patients with dysferlinopathy were classified by initial muscle weakness: fifteen patients with Miyoshi myopathy phenotype (MM), thirteen patients with limb girdle muscular dystrophy 2B phenotype (LGMD2B), two patients with proximodistal phenotype, and one asymptomatic patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793917.RA3OYAJY0gaD7ugAdMCi-7F-Sj4CsrBJuyMHeYbvbIdTc130_provenance.