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- NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_assertion type Assertion NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_head.
- NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_assertion wasGeneratedBy ECO_0000203 NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_provenance.
- NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_assertion wasDerivedFrom gad-20130706 NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_provenance.
- NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_assertion SIO_000772 19027966 NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_provenance.
- NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_assertion evidence source_evidence_literature NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_provenance.
- NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_assertion description "[In the years 2005-2007 we have screened 194 probands with early onset hearing loss and 68 family members with an arrayed primer extension (APEX) microarray, which covers 201 mutations in six nuclear genes (GJB2, GJB6, GJB3, GJA1, SLC26A4, SLC26A5) and two mitochondrial genes encoding 12S rRNA and tRNA-Ser (UCN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74432.RARSSyNt19UD2NNEQhCXQv-rzsVcrMaEnP3RoURW1gDM8130_provenance.