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- source_evidence_literature type ECO_0000212 NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- befree-2016 importedOn "2016-02-19" NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_assertion wasGeneratedBy ECO_0000203 NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_assertion wasDerivedFrom befree-2016 NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_assertion SIO_000772 11561226 NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_assertion evidence source_evidence_literature NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.
- NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_assertion description "[Novel rod segment mutations in lamin A/C cause variable conduction system disease and dilated cardiomyopathy without skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330437.RAQop_KDQSWdv2WhG7uUkCzzSxBtro_6Kn_0C0DGSixIY130_provenance.