Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.