Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_assertion description "[This study evaluated common clinical characteristics of patients with lamin A/C gene mutations that cause either isolated dilated cardiomyopathy or dilated cardiomyopathy in association with skeletal muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_assertion evidence source_evidence_literature NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_assertion SIO_000772 15551023 NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_assertion wasDerivedFrom befree-2016 NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_assertion wasGeneratedBy ECO_0000203 NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.
- befree-2016 importedOn "2016-02-19" NP469574.RAcXPW2krVyXs2jfchpCPUZ11Z6pqDVrKIzp7hKyU711w130_provenance.