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- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion type Assertion NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_head.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion evidence source_evidence_literature NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion SIO_000772 24767429 NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion wasDerivedFrom befree-20150227 NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion wasGeneratedBy ECO_0000203 NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.