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- source_evidence_literature type ECO_0000212 NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_assertion description "[The occurrence of this chromosomal abnormality reinforces the concept of tumour suppressor gene hypothesis in some cases with familial MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_assertion evidence source_evidence_literature NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_assertion SIO_000772 8217806 NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_assertion wasDerivedFrom befree-20150227 NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_assertion wasGeneratedBy ECO_0000203 NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP758733.RAG_sP5QkTxYPVjgsBB0cXJeMMKl2phbfW-pwyWKntQJs130_provenance.