Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion> ?p ?o ?g. }
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- NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion type Assertion NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_head.
- NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion description "[The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_provenance.
- NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion evidence source_evidence_literature NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_provenance.
- NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion SIO_000772 20801718 NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_provenance.
- NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion wasDerivedFrom gad-20150221 NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_provenance.
- NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion wasGeneratedBy ECO_0000203 NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_provenance.