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- source_evidence_literature type ECO_0000212 NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_assertion description "[The concomitant 1p partial loss and chromosome 19 alterations, with the +7 and -10-specific GBM markers associated with homozygous deletion of 9p21.3 including CDKN2A (p16), are distinct features of the glioblastoma MI-4 cell line, illustrating its origin from an olidodendroglial tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_assertion evidence source_evidence_literature NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_assertion SIO_000772 16102584 NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_assertion wasDerivedFrom befree-2016 NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_assertion wasGeneratedBy ECO_0000203 NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.
- befree-2016 importedOn "2016-02-19" NP508922.RAZ70PUCxCuUBTOB8c4DHA2AAIaXJI4aKPbv5gL96lHsM130_provenance.