Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_assertion description "[The coincidence of chromosome 15 aberrations and beta2-microglobulin gene mutations is causative for the total loss of human leukocyte antigen class I expression in melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_assertion evidence source_evidence_literature NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_assertion SIO_000772 16740750 NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_assertion wasDerivedFrom befree-20150227 NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_assertion wasGeneratedBy ECO_0000203 NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP456657.RABNtmY1TmCM68mC_U4qiir4bEKlZm_YzpG1230Z47pwo130_provenance.