Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_assertion wasGeneratedBy ECO_0000203 NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_assertion wasDerivedFrom befree-2016 NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_assertion SIO_000772 22838948 NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_assertion evidence source_evidence_literature NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.
- NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_assertion description "[Children with ALL (n = 96) were screened for GCPII C1561T, RFC1 G80A, cSHMT C1420T, TYMS 5´-UTR 2R3R, TYMS 3´-UTR ins6/del6, MTHFR C677T, MTR A2756G polymorphisms using PCR-RFLP and PCR-amplified fragment length polymorphism techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1000759.RApznjRAiR2NeAuObGZiWBF6YzYt8mxK6J_GDGJb5gHGI130_provenance.