Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_assertion description "[Three of the four FGFR1-rearranged cases were associated with myeloproliferative neoplasms but none, including the two with sole 8p11.2, displayed the typical phenotype for stem cell leukemia/lymphoma (SCLL) and only one had eosinophilia; the fourth case had AML-M4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_assertion evidence source_evidence_literature NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_assertion SIO_000772 20143402 NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_assertion wasDerivedFrom befree-20140225 NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_assertion wasGeneratedBy ECO_0000203 NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490624.RAxipq82aY0jk2DkQe6aDL2ji2Ii33VucSxepzzBNeQkQ130_provenance.