Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_assertion evidence source_evidence_literature NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_assertion SIO_000772 8162055 NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_assertion wasDerivedFrom befree-20150227 NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_assertion wasGeneratedBy ECO_0000203 NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.