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- NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_assertion type Assertion NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_head.
- NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_assertion wasGeneratedBy ECO_0000203 NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_provenance.
- NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_assertion wasDerivedFrom befree-20150227 NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_provenance.
- NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_assertion SIO_000772 17234811 NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_provenance.
- NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_assertion evidence source_evidence_literature NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_provenance.
- NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_assertion description "[The family also was screened for mutations in cadherin 23, which accentuated hearing loss in a previously described human family with a PMCA2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256529.RAVxqkrr7iyZsJ0aFBsuw4MWz61lKNgeetcD7_jJMWrSg130_provenance.