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- source_evidence_literature type ECO_0000212 NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_assertion description "[A variant located at the 3' UTR of the FGF2 gene (rs6820411) was highly associated with atrophic AMD, and the functional SNP rs3112831 at ABCA4 showed a marginal association with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_assertion evidence source_evidence_literature NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_assertion SIO_000772 21106043 NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_assertion wasDerivedFrom befree-2016 NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_assertion wasGeneratedBy ECO_0000203 NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
- befree-2016 importedOn "2016-02-19" NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.