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- source_evidence_literature type ECO_0000212 NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_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." NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_assertion evidence source_evidence_literature NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_assertion SIO_000772 22182939 NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_assertion wasDerivedFrom befree-2016 NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_assertion wasGeneratedBy ECO_0000203 NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.
- befree-2016 importedOn "2016-02-19" NP947913.RAN3mCT6SUa1a3KKzg4dZtL3ank4TYCCa283nCuMye4Hg130_provenance.