Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_assertion wasGeneratedBy ECO_0000203 NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_assertion wasDerivedFrom befree-20140225 NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_assertion SIO_000772 9264367 NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_assertion evidence source_evidence_literature NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_assertion description "[Deletions of the long arm of chromosome 5 with common overlapping segment 5q31.1 are among the most frequent cytogenetic aberrations in myelodysplastic syndromes and acute myeloid leukemias (MDS/AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP268456.RAVOqEfYIO0i-ahb7W4F2kVZSKK1p_xjbeLoOOVH0FQsM130_provenance.