Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_assertion description "[All GJB2 mutations were associated with prelingual hearing loss, though severity ranged from moderate to profound, with variability even among hearing impaired siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_assertion evidence source_evidence_literature NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_assertion SIO_000772 10982182 NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_assertion wasDerivedFrom befree-2016 NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_assertion wasGeneratedBy ECO_0000203 NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.
- befree-2016 importedOn "2016-02-19" NP294743.RAo1yAUeds1_ILDAVhpHC3V5suUpxDq3EQp5Y9VyhIiMs130_provenance.