Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_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." NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_assertion evidence source_evidence_literature NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_assertion SIO_000772 7790377 NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_assertion wasDerivedFrom befree-20140225 NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_assertion wasGeneratedBy ECO_0000203 NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505387.RABjCcPstggiiEtL_bMetC1jG_eE4gBqatKeO2IECLiDs130_provenance.