Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_assertion description "[These mutant mice did not recapture the abnormal phenotype observed in the human patient but displayed a mild rachitic tooth phenotype in comparison with that in the Dmp1-null mice, suggesting that the DI III-like phenotype may be due to an as-yet-undetermined acquired gene modifier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_assertion evidence source_evidence_literature NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_assertion SIO_000772 20499360 NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_assertion wasDerivedFrom befree-2016 NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_assertion wasGeneratedBy ECO_0000203 NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.
- befree-2016 importedOn "2016-02-19" NP814404.RARpDfTfOoNnxP37dOTzoEcPT7EiA7gh9PBiFVdSRrGAc130_provenance.