Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_assertion> ?p ?o ?g. }
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- NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_assertion type Assertion NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_head.
- NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_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." NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.
- NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_assertion evidence source_evidence_literature NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.
- NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_assertion SIO_000772 20031618 NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.
- NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_assertion wasDerivedFrom gad-20150221 NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.
- NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_assertion wasGeneratedBy ECO_0000203 NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.