Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_assertion description "[The FRA2C common fragile site maps to the borders of MYCN amplicons in neuroblastoma and is associated with gross chromosomal rearrangements in different cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_assertion evidence source_evidence_literature NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_assertion SIO_000772 21258086 NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_assertion wasDerivedFrom befree-20150227 NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_assertion wasGeneratedBy ECO_0000203 NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP411350.RANsqM0IvhNvlHDYrpWn7Q-rJJ_cWdlMDm_BI9iBe-CUY130_provenance.