Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion wasGeneratedBy ECO_0000218 NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion wasDerivedFrom uniprot-20150221 NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion SIO_000772 20137778 NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion evidence source_evidence_curated NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- 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.