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- source_evidence_literature type ECO_0000212 NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_assertion description "[Homozygous mutations in the MYBPC3 gene have been identified as the cause of severe infantile HCM among the Amish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_assertion evidence source_evidence_literature NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_assertion SIO_000772 18467358 NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_assertion wasDerivedFrom befree-20150227 NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_assertion wasGeneratedBy ECO_0000203 NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP580943.RAE8Gp6e39R0OP3_hmhZz9lL5ySyrKDJw3LjU1icdid5E130_provenance.