Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_assertion> ?p ?o ?g. }
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- NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_assertion type Assertion NP16858.RARVxtlKp40elCDvu-eurtHoH7yaispJA4YKAZZMaAA2c130_head.
- 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.