Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_assertion description "[The tip links that organize the bundle are formed by the Ca(2+) binding protein cadherin 23 and by protocadherin 15: Disturbances of the Ca(2+) binding by cadherin 23 and/or of the ability of the PMCA2 variant of the stereocilia to export Ca(2+) to the endolymph generate hearing loss phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_assertion evidence source_evidence_literature NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_assertion SIO_000772 21786191 NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_assertion wasDerivedFrom befree-2016 NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_assertion wasGeneratedBy ECO_0000203 NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.
- befree-2016 importedOn "2016-02-19" NP912000.RAG2R-zGzBlbdLNDvXxKhrHqgLSXl1MGqk0UUTTrZzkPE130_provenance.