Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_assertion> ?p ?o ?g. }
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- NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_assertion type Assertion NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_head.
- NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_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." NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_provenance.
- NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_assertion evidence source_evidence_literature NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_provenance.
- NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_assertion SIO_000772 14740321 NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_provenance.
- NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_assertion wasDerivedFrom befree-2016 NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_provenance.
- NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_assertion wasGeneratedBy ECO_0000203 NP429286.RADMHQsVREZCGUOOPIdI2Xlu3OsPrzjWIdlQkx4BiQhOE130_provenance.