Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_assertion wasGeneratedBy ECO_0000218 NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_assertion wasDerivedFrom ctd_human-2016 NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_assertion SIO_000772 16385454 NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_assertion evidence source_evidence_curated NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.
- NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_assertion description "[Mutational spectrum of D-bifunctional protein deficiency and structure-based genotype-phenotype analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_provenance.