Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_assertion description "[Frequencies of Six (Five Novel) STR Markers Linked to TUSC3 (MRT7) or NSUN2 (MRT5) Genes Used for Homozygosity Mapping of Recessive Intellectual Disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_assertion evidence source_evidence_literature NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_assertion SIO_000772 26427135 NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_assertion wasDerivedFrom befree-2016 NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_assertion wasGeneratedBy ECO_0000203 NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294613.RA14GRhnHp7KIBJz5OYS_p5YpTJ2gwTB-cV-PXW22pqTM130_provenance.