Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion> ?p ?o ?g. }
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- NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion type Assertion NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_head.
- NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_provenance.
- NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion evidence source_evidence_curated NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_provenance.
- NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion SIO_000772 23559863 NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_provenance.
- NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion wasDerivedFrom uniprot-2016 NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_provenance.
- NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion wasGeneratedBy ECO_0000218 NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_provenance.