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- source_evidence_literature type ECO_0000212 NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_assertion description "[The evidence for this assertion is strongest in Parkinson's disease (PD), where genetic variability in alpha-synuclein expression affects risk of developing disease, although the oldest evidence for the notion that increased expression of normal sequence protein can lead to disease comes from the observation of Alzheimer's disease in trisomy 21 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_assertion evidence source_evidence_literature NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_assertion SIO_000772 14976159 NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_assertion wasDerivedFrom befree-20150227 NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_assertion wasGeneratedBy ECO_0000203 NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788059.RAYUvRTG-XiQEwzMqWW6IGYXZHqyYIaywAHsrcMDQieTk130_provenance.