Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_assertion evidence source_evidence_literature NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_assertion SIO_000772 15596616 NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_assertion wasDerivedFrom befree-20140225 NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_assertion wasGeneratedBy ECO_0000203 NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.