Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_assertion> ?p ?o ?g. }
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- NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_assertion type Assertion NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_head.
- NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_assertion description "[Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_provenance.
- NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_assertion evidence source_evidence_curated NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_provenance.
- NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_assertion SIO_000772 25633957 NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_provenance.
- NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_assertion wasDerivedFrom uniprot-2016 NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_provenance.
- NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_assertion wasGeneratedBy ECO_0000218 NP8132.RAR52t5pIry1fFIZrEsNQmUq-ELqpvkx9B4v3OMi-6qTo130_provenance.