Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_assertion description "[Phenotype in GJB2-associated hearing loss is correlated with genotype, with truncating mutations giving rise to more severe hearing loss. Progression of hearing loss is not uncommon, especially in association with the p.V37I allele. These results suggest ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_assertion evidence source_evidence_literature NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_assertion SIO_000772 20154630 NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_assertion wasDerivedFrom gad-20150221 NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_assertion wasGeneratedBy ECO_0000203 NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP138147.RACLma3Se9RoQe1JPuGiPdAjJg9zizEq3j4gHPsT5Rox4130_provenance.