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- source_evidence_literature type ECO_0000212 NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_assertion description "[Mutation of the MYH7 gene in a child with hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_assertion evidence source_evidence_literature NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_assertion SIO_000772 17495353 NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_assertion wasDerivedFrom befree-20150227 NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_assertion wasGeneratedBy ECO_0000203 NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583316.RA62HMrPVZXdQj8Igt0anARbB6k1HjgVHkHHsttRegWec130_provenance.