Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_assertion description "[Notably, the human ABCG1 gene maps to chromosome 21q22.3, and individuals with Down syndrome (DS) typically manifest with Alzheimer's disease (AD) neuropathology in their 30s.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_assertion evidence source_evidence_literature NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_assertion SIO_000772 17293612 NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_assertion wasDerivedFrom befree-20140225 NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_assertion wasGeneratedBy ECO_0000203 NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.