Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_assertion evidence source_evidence_literature NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_assertion SIO_000772 19061983 NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_assertion wasDerivedFrom befree-20140225 NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_assertion wasGeneratedBy ECO_0000203 NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.
- befree-20140225 importedOn "2014-02-25" NP880211.RAxVaWkf9j159yAUsKKklDtSgdB-PSx4K5kV5YI-xuJps130_provenance.