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- source_evidence_literature type ECO_0000212 NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_assertion description "[Our results show that BRAF mutation can also be present in CCS and support the proposed aberration of chromosomes 22 and 8 as a possibly useful nonrandom hallmark of EWSR1- CCS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_assertion evidence source_evidence_literature NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_assertion SIO_000772 22045652 NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_assertion wasDerivedFrom befree-20150227 NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_assertion wasGeneratedBy ECO_0000203 NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387982.RAuqSt7XaAhRlD-Krpye5P0JOhNRk-0IyLN-yzrDMy3Cw130_provenance.