Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_assertion description "[Cases of FCD types Ia (13) and IIb (4), pediatric hippocampal sclerosis (HS) (5), temporal lobe sclerosis (5), glioneuronal tumors (5), gray matter heterotopia (3), and control tissues (16) from a wide age range [20 gestational weeks (GW) to 85 years] were studied using immunohistochemistry to DCX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_assertion evidence source_evidence_literature NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_assertion SIO_000772 19583780 NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_assertion wasDerivedFrom befree-20140225 NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_assertion wasGeneratedBy ECO_0000203 NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP769680.RApstqU-OB4IhJflQ7fTnSG9YGoVOtLB7a4XuuK_iB2rs130_provenance.