Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_assertion description "[These have recently included those that encode skeletal muscle alpha-actin in autosomal dominant and autosomal recessive nemaline myopathy, nebulin and slow alpha-tropomyosin in autosomal recessive nemaline myopathy, and desmin and alpha B-crystallin in desminopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_assertion evidence source_evidence_literature NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_assertion SIO_000772 10590887 NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_assertion wasDerivedFrom befree-20140225 NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_assertion wasGeneratedBy ECO_0000203 NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP195001.RAfKLijZk9TdBoVNdLsFfhGKweoQiuRP4vc3tqKWGCsOk130_provenance.