Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_assertion> ?p ?o ?g. }
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- NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_assertion type Assertion NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_head.
- NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_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." NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_provenance.
- NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_assertion evidence source_evidence_literature NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_provenance.
- NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_assertion SIO_000772 20031618 NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_provenance.
- NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_assertion wasDerivedFrom gad-20150221 NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_provenance.
- NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_assertion wasGeneratedBy ECO_0000203 NP88091.RA84zFc3IAvk7hK5c0VIjs0u6-iKP44NhN0OxSf0lBlcE130_provenance.