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- source_evidence_literature type ECO_0000212 NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP580895.RAnh86dwwqEoiTpfXSN9keHT8BieINSq6P3PQTtd1jEmg130_provenance.