Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion> ?p ?o ?g. }
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- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion type Assertion NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_head.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion description "[Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes (USH2A, USH2B, and USH2C) and is classified phenotypically as congenital hearing loss and progressive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion evidence source_evidence_literature NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion SIO_000772 14740321 NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion wasDerivedFrom befree-20140225 NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.
- NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_assertion wasGeneratedBy ECO_0000203 NP345231.RASfzcMv8rD-EUCoCgXXJ5BpiX-zSviTsh9yez1aJt8Lg130_provenance.