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- NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_assertion type Assertion NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_head.
- NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_provenance.
- NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_assertion evidence source_evidence_literature NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_provenance.
- NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_assertion SIO_000772 21480433 NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_provenance.
- NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_assertion wasDerivedFrom befree-20150227 NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_provenance.
- NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_assertion wasGeneratedBy ECO_0000203 NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_provenance.