Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_assertion type Assertion NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_head.
- NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_assertion description "[Furthermore, mutations in the PMP70 gene have also been identified in two Zellweger syndrome patients from CG1, raising the possibility that CG1 patients may represent a mixture of PEX1-deficient and PMP70-deficient individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_provenance.
- NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_assertion evidence source_evidence_curated NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_provenance.
- NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_assertion SIO_000772 10447258 NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_provenance.
- NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_assertion wasDerivedFrom ctd_human-20130708 NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_provenance.
- NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_assertion wasGeneratedBy ECO_0000218 NP25751.RAz5L0A1cXt2rvRckIz0gN5xXlP34Jtx2sD0PkBvsypEo130_provenance.