Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_assertion description "[Exploring the (CAG)n expansion within IT 15 gene in Turkish Huntington's disease (HD) patients and its relation to downstream (CCG)n repeat polymorphism to elucidate population specific haplotypic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_assertion evidence source_evidence_literature NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_assertion SIO_000772 10478585 NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_assertion wasDerivedFrom befree-2016 NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_assertion wasGeneratedBy ECO_0000203 NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.
- befree-2016 importedOn "2016-02-19" NP262402.RACg5XxUslyV7s5eihB824VVwOv4zJjbowFQLSfOUHpqU130_provenance.