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- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion type Assertion NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_head.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion description "[In all, 68 children with nonsyndromic sensorineural hearing loss were screened for Cx26 and Cx30 mutations by polymerase chain reaction and direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion evidence source_evidence_literature NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion SIO_000772 15064611 NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion wasDerivedFrom befree-2016 NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion wasGeneratedBy ECO_0000203 NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.