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- source_evidence_literature type ECO_0000212 NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_assertion description "[Huntington disease is a neurodegenerative disorder caused by a CAG repeat amplification in the gene huntingtin (HTT) that is reflected by a polyglutamine expansion in the Htt protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_assertion evidence source_evidence_literature NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_assertion SIO_000772 22556411 NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_assertion wasDerivedFrom befree-2016 NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_assertion wasGeneratedBy ECO_0000203 NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.
- befree-2016 importedOn "2016-02-19" NP979626.RAsecX2ve8z43qEfPW3-wwCg5BsF_JgAw1KStaAVrKMbs130_provenance.