Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_assertion> ?p ?o ?g. }
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- NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_assertion type Assertion NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_head.
- NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_assertion description "[C9orf72 mutations are the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_provenance.
- NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_assertion evidence source_evidence_literature NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_provenance.
- NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_assertion SIO_000772 26308983 NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_provenance.
- NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_assertion wasDerivedFrom befree-2016 NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_provenance.
- NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_assertion wasGeneratedBy ECO_0000203 NP1293231.RAdqZfphGrQZM551lFSfQ5WHWI_HxqIdiRvQopx26D4pY130_provenance.