Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion description "[Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are the most common known genetic cause of frontotemporal dementia (FTD) and motor neuron disease (MND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion evidence source_evidence_literature NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion SIO_000772 24011653 NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion wasDerivedFrom befree-20140225 NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion wasGeneratedBy ECO_0000203 NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.