Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_assertion> ?p ?o ?g. }
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- NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_assertion type Assertion NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_head.
- NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_assertion wasGeneratedBy ECO_0000203 NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_provenance.
- NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_assertion wasDerivedFrom befree-2016 NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_provenance.
- NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_assertion SIO_000772 11558900 NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_provenance.
- NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_assertion evidence source_evidence_literature NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_provenance.
- NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_assertion description "[Genetic features of hearing loss associated with ear anomalies: PDS and EYA1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330248.RAPOmPCpjm1-wCOXeNv1eTPnRKaxBuXWEkDtTbWx3Y6P8130_provenance.