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- NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_assertion type Assertion NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_head.
- NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_assertion wasGeneratedBy ECO_0000203 NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_provenance.
- NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_assertion wasDerivedFrom befree-20150227 NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_provenance.
- NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_assertion SIO_000772 17234811 NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_provenance.
- NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_assertion evidence source_evidence_literature NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_provenance.
- NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_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." NP936897.RADLVE8Rii4zNY60AoJKl09K_DXzQqCpNQCEYuz2YBNZE130_provenance.