Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_assertion> ?p ?o ?g. }
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- NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_assertion type Assertion NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_head.
- NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_assertion description "[Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_provenance.
- NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_assertion evidence source_evidence_literature NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_provenance.
- NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_assertion SIO_000772 21940737 NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_provenance.
- NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_assertion wasDerivedFrom befree-2016 NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_provenance.
- NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_assertion wasGeneratedBy ECO_0000203 NP925806.RAKvKQrXBdBney-hIJsuZeEc7MzpQ2pvY9O9e1c4XbKQw130_provenance.