Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_assertion description "[Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_assertion evidence source_evidence_literature NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_assertion SIO_000772 22182939 NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_assertion wasDerivedFrom befree-20140225 NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_assertion wasGeneratedBy ECO_0000203 NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP375954.RAywF0ef1znnw07b5d08Qq8tY3cEcZqEL_cTN2NcwpPCk130_provenance.