Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_assertion description "[Taken together, our data indicate that PRKAG2 mutations do not cause hypertrophic cardiomyopathy but rather lead to a novel myocardial metabolic storage disease, in which hypertrophy, ventricular pre-excitation and conduction system defects coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_assertion evidence source_evidence_literature NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_assertion SIO_000772 11827995 NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_assertion wasDerivedFrom befree-2016 NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_assertion wasGeneratedBy ECO_0000203 NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.
- befree-2016 importedOn "2016-02-19" NP344058.RAdWKxY29K8C5tILMp3WpkvMHlCFnDnqwYNHbQY0l9bHs130_provenance.