Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_assertion description "[Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_assertion evidence source_evidence_literature NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_assertion SIO_000772 16757412 NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_assertion wasDerivedFrom befree-20140225 NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_assertion wasGeneratedBy ECO_0000203 NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP600139.RADKFm7ryLTSwF3VgzX5Sl2cz-aiprJXcoswjMkZdxq-Q130_provenance.