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- source_evidence_literature type ECO_0000212 NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP161749.RAh-uNqPG3L9F8ujwdvMkG1CwajRJJL4qbehftOp19f_0130_provenance.