Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion evidence source_evidence_curated NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion SIO_000772 24767429 NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion wasDerivedFrom uniprot-2016 NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion wasGeneratedBy ECO_0000218 NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.