Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_assertion description "[A high frequency of epilepsy (43%) was observed in our patients with GLUD1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_assertion evidence source_evidence_literature NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_assertion SIO_000772 19690084 NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_assertion wasDerivedFrom befree-20140225 NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_assertion wasGeneratedBy ECO_0000203 NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP842859.RA7H02LZQgKTf2NMhD4nlh5pFAFQn3-nBu8zzRHlAP2B8130_provenance.