Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion> ?p ?o ?g. }
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- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion type Assertion NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_head.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion evidence source_evidence_curated NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion SIO_000772 20137778 NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion wasDerivedFrom uniprot-20150221 NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion wasGeneratedBy ECO_0000218 NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.