Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_assertion description "[Hexanucleotide expansion repeats in the C9ORF72 gene are a major cause of familial and, to a lesser extent, sporadic frontotemporal lobar degeneration (FTLD), amyotrophic lateral sclerosis (ALS), and FTLD-ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_assertion evidence source_evidence_literature NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_assertion SIO_000772 22766732 NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_assertion wasDerivedFrom befree-2016 NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_assertion wasGeneratedBy ECO_0000203 NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.
- befree-2016 importedOn "2016-02-19" NP995476.RAZY3lV8Qsi3YrmR_XCzBZfan9snMbM-v9Z7AmSzWo2MM130_provenance.