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- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion type Assertion NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_head.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion description "[Mutations in the Connexin 26 (Cx26) gene have been found to account for approximately 20% of all childhood deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion evidence source_evidence_literature NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion SIO_000772 12121355 NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion wasDerivedFrom befree-20150227 NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.
- NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_assertion wasGeneratedBy ECO_0000203 NP426339.RANqgaq6nazeO_jvIxzt5tEWSytrvucKuVwKEaqjNF1ow130_provenance.