Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_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 dementia provides further evidence of a shared genetic cause for these two neurodegenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_assertion evidence source_evidence_literature NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_assertion SIO_000772 20801718 NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_assertion wasDerivedFrom gad-20130706 NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_assertion wasGeneratedBy ECO_0000203 NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP51235.RAIK6JYlA7xwf3Gej6LTbn6j7LAHir101F8MfyKuKH0yE130_provenance.