Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_assertion wasGeneratedBy ECO_0000203 NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_assertion wasDerivedFrom befree-20150227 NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_assertion SIO_000772 16242644 NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_assertion evidence source_evidence_literature NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.
- NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_assertion description "[Constitutive Dyrk1A is abnormally expressed in Alzheimer disease, Down syndrome, Pick disease, and related transgenic models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362673.RA2CYIiVoouPYDqr1iPOMUIs_eo7EQr3vxA5RGL0HY2eY130_provenance.