Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_assertion description "[In addition, mutations in lamin A/C can give rise to a dilated cardiomyopathy, a lipodystrophy or a neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_assertion evidence source_evidence_literature NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_assertion SIO_000772 14585157 NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_assertion wasDerivedFrom befree-2016 NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_assertion wasGeneratedBy ECO_0000203 NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.
- befree-2016 importedOn "2016-02-19" NP418673.RAYhblkcfKDh_Td8ueJMlzXfl-7mHQ5NEhGf_Pxgt1snU130_provenance.