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- source_evidence_literature type ECO_0000212 NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_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." NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_assertion evidence source_evidence_literature NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_assertion SIO_000772 20801718 NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_assertion wasDerivedFrom gad-20130706 NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_assertion wasGeneratedBy ECO_0000203 NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP82496.RAjNJFOw6f3fSdkp14uKKeNlZrfsIMNm0x5Y2wBG5usOI130_provenance.