Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_assertion description "[This study shows that familial disease is common among infants and children with HCM and that, in most cases, disease is caused by mutations in cardiac sarcomere protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_assertion evidence source_evidence_literature NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_assertion SIO_000772 20031618 NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_assertion wasDerivedFrom gad-20150221 NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_assertion wasGeneratedBy ECO_0000203 NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.
- gad-20150221 importedOn "2015-02-21" NP161759.RAQkWCgC6X_qo_GieaRyeAZV5U1jibhXeK7hIgHXiIK9M130_provenance.