Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_assertion> ?p ?o ?g. }
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- NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_assertion type Assertion NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_head.
- NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_assertion description "[The PTS1R cDNA also complements the PTS1 protein-import defect in skin fibroblasts from patients--belonging to complementation group two--diagnosed as having neonatal adrenoleukodystrophy or Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_provenance.
- NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_assertion evidence source_evidence_literature NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_provenance.
- NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_assertion SIO_000772 7790377 NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_provenance.
- NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_assertion wasDerivedFrom befree-2016 NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_provenance.
- NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_assertion wasGeneratedBy ECO_0000203 NP1321913.RAyxGjzVOBhLKrIL2DStCs1ZvRzHP7gr2a0YGI6Ip-Wu0130_provenance.