Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion> ?p ?o ?g. }
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- NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion type Assertion NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_head.
- 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.