Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion> ?p ?o ?g. }
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- NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion type Assertion NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_head.
- NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion description "[We identified a c.1625G > T mutation in exon 12 of COCH that co-segregates with auditory dysfunction in the pedigree.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.
- NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion evidence source_evidence_literature NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.
- NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion SIO_000772 16261627 NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.
- NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion wasDerivedFrom befree-20150227 NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.
- NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion wasGeneratedBy ECO_0000203 NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.