Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_assertion description "[5' (bcr 3) breakpoints in PML were over represented among the group and three patients had complex cytogenetic abnormalities suggesting both factors may increase the risk of relapse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_assertion evidence source_evidence_literature NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_assertion SIO_000772 8558940 NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_assertion wasDerivedFrom befree-20150227 NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_assertion wasGeneratedBy ECO_0000203 NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1004752.RAARkbbsVUYRxPgm9ZycHtNzY6VXN_Y_FvppTQn0yt5Sg130_provenance.