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- source_evidence_literature type ECO_0000212 NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_assertion description "[For example, mice with a functionally significant mutation of Brain-4, which is expressed in the connective tissue cells within the cochlea, show marked depression of the endolymphatic potential and profound sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_assertion evidence source_evidence_literature NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_assertion SIO_000772 11810458 NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_assertion wasDerivedFrom befree-2016 NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_assertion wasGeneratedBy ECO_0000203 NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.
- befree-2016 importedOn "2016-02-19" NP343267.RABt9g2klmxliXWclkawDdC9z-L-OkShseJ10Fy1Gl6gI130_provenance.