Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_assertion description "[Malignant mutation in lamin A/C gene causing progressive conduction system disease and early death in limb-girdle muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_assertion evidence source_evidence_literature NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_assertion SIO_000772 17605093 NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_assertion wasDerivedFrom lhgdn-20090331 NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_assertion wasGeneratedBy ECO_0000203 NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP208589.RAH3Cx74gk67iSHWOQLowa60lhqiKTZN7eZqy3WYZo3rQ130_provenance.