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- source_evidence_literature type ECO_0000212 NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_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." NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_assertion evidence source_evidence_literature NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_assertion SIO_000772 7790377 NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_assertion wasDerivedFrom befree-2016 NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_assertion wasGeneratedBy ECO_0000203 NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1321915.RAGcpTCO3Bidgft-6ItWPVhOAQ51jFauG3pwo2A8QPfEo130_provenance.