Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_assertion description "[Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_assertion evidence source_evidence_literature NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_assertion SIO_000772 10431236 NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_assertion wasDerivedFrom befree-20140225 NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_assertion wasGeneratedBy ECO_0000203 NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP680363.RAE8Z9T9JLOsHZelnZreCgmiCGD4OalcV2gnLTGSKA1U4130_provenance.