Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_assertion> ?p ?o ?g. }
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- NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_assertion type Assertion NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_head.
- NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_assertion description "[Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease and is often a consequence of mutations in the myosin-binding protein C gene (MYBPC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.
- NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_assertion evidence source_evidence_literature NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.
- NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_assertion SIO_000772 16566405 NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.
- NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_assertion wasDerivedFrom befree-20150227 NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.
- NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_assertion wasGeneratedBy ECO_0000203 NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.