Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_assertion type Assertion NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_head.
- NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_assertion description "[Furthermore, detailed analysis of PXR1 has revealed that mutations in this gene are responsible for complementation group 2 of the peroxisome biogenesis disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_provenance.
- NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_assertion evidence source_evidence_literature NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_provenance.
- NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_assertion SIO_000772 8993569 NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_provenance.
- NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_assertion wasDerivedFrom befree-20140225 NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_provenance.
- NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_assertion wasGeneratedBy ECO_0000203 NP616634.RADCtSR9Wew-BG_IY29PSBRKmfiT7p54E-uqqoqXh5OIE130_provenance.