Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_assertion description "[We report on a patient who had carried a clinical diagnosis of PDE for 7 years, but who was than shown to have normal ALDH7A1 sequencing and the absence of biomarkers characteristic of this familial epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_assertion evidence source_evidence_literature NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_assertion SIO_000772 23166088 NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_assertion wasDerivedFrom befree-2016 NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_assertion wasGeneratedBy ECO_0000203 NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1029707.RAZ7z1X1UF_x7MVQgvBE0G6egoTzPGqcIFvsXY1ePV9Fc130_provenance.