Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_assertion description "[Novel LMNA mutation presenting as severe congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_assertion evidence source_evidence_literature NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_assertion SIO_000772 20837309 NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_assertion wasDerivedFrom befree-20150227 NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_assertion wasGeneratedBy ECO_0000203 NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537778.RANyZEN-WNMJozrWGY0NNdNBvGlq9VyxzLEXGPkKdUY7E130_provenance.