Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_assertion description "[A novel desmin R355P mutation has been identified in a patient with familial cardiac and skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_assertion evidence source_evidence_literature NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_assertion SIO_000772 16009553 NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_assertion wasDerivedFrom lhgdn-20090331 NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_assertion wasGeneratedBy ECO_0000203 NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198162.RAVWLNgITQoPaF98sVdW3J4UCUrdxw4ixO-vINOvxfPFw130_provenance.