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- source_evidence_literature type ECO_0000212 NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_assertion description "[The fact that our linkage region 1p36 overlaps with the dyslexia QTL DYX8 further suggests it is potentially a pleiotropic locus for ADHD and dyslexia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_assertion evidence source_evidence_literature NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_assertion SIO_000772 18439570 NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_assertion wasDerivedFrom befree-20150227 NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_assertion wasGeneratedBy ECO_0000203 NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP992207.RAgRd53VYBIw-R7rvP-ES09xBAjX4LbaYkZXG-AVq9DHE130_provenance.