Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_assertion> ?p ?o ?g. }
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- NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_assertion type Assertion NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_head.
- NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_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." NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_provenance.
- NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_assertion evidence source_evidence_literature NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_provenance.
- NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_assertion SIO_000772 20801718 NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_provenance.
- NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_assertion wasDerivedFrom gad-20150221 NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_provenance.
- NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_assertion wasGeneratedBy ECO_0000203 NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_provenance.