Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_assertion description "[With in the TD group, we could not discover a significant correlation between NOS1 3'-UTR C276T genotypes and the scores of abnormal involuntary movement scale (AIMS) (p=0.219 and 0.774).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_assertion evidence source_evidence_literature NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_assertion SIO_000772 15088155 NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_assertion wasDerivedFrom befree-20140225 NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_assertion wasGeneratedBy ECO_0000203 NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP864058.RA_s0Rtqyqxm-V0_iQPchzfID8Nc1p-ogsJ_DsCuEfdlg130_provenance.