Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion> ?p ?o ?g. }
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- NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion type Assertion NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_head.
- NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_provenance.
- NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion evidence source_evidence_literature NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_provenance.
- NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion SIO_000772 25467142 NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_provenance.
- NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion wasDerivedFrom befree-2016 NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_provenance.
- NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion wasGeneratedBy ECO_0000203 NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_provenance.