Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_assertion description "[Two hundred and twenty-three consecutive patients fulfilling clinical diagnostic criteria for frontotemporal lobar degeneration (FTLD), and 259 patients with motor neuron disease (MND), for whom genomic DNA was available, were investigated for the presence of mutations in tau (MAPT) and progranulin (PGRN) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_assertion evidence source_evidence_literature NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_assertion SIO_000772 18192287 NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_assertion wasDerivedFrom befree-2016 NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_assertion wasGeneratedBy ECO_0000203 NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP649606.RApicvHT0tIaBA6NZY1-tYne4otakTJJInhqygpUeSiLQ130_provenance.