Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion> ?p ?o ?g. }
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- NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion type Assertion NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_head.
- 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.