Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_assertion description "[Missense mutations in two related genes, termed presenilin 1 (PS1) and presenilin 2 (PS2), cause dementia in a subset of early-onset familial Alzheimer's disease (FAD) pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_assertion evidence source_evidence_literature NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_assertion SIO_000772 9354339 NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_assertion wasDerivedFrom befree-20140225 NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_assertion wasGeneratedBy ECO_0000203 NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316609.RAACrCLgIK7DZ5Y_GpceU-iqs4FVXIjbNDsMVmVI5G-Wk130_provenance.