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- source_evidence_literature type ECO_0000212 NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_assertion description "[One such patient had a complex chromosomal abnormality, leading to the identification of a fusion of the Fip1-like 1 (FIP1L1) gene to the PDGFRalpha (PDGFRA) gene generated by an interstitial deletion on chromosome 4q12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_assertion evidence source_evidence_literature NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_assertion SIO_000772 12660384 NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_assertion wasDerivedFrom befree-20140225 NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_assertion wasGeneratedBy ECO_0000203 NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP820824.RAOTio_16BtnbtY5nJF1a3jTI58ifMpe53reFFQqHqF-k130_provenance.