Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_assertion description "[Class I and Class II mutations are significantly associated, indicating their cooperation in leukemogenesis The chromosome aberrations and gene mutations detected in the therapy-related and in the de novo subsets of MDS and AML are identical, although the frequencies with which they are observed may differ.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_assertion evidence source_evidence_literature NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_assertion SIO_000772 18024656 NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_assertion wasDerivedFrom befree-20150227 NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_assertion wasGeneratedBy ECO_0000203 NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978436.RA1tdTM7AICFc34XcoK8iCNasjxhczGd-lQHLWQhzGT4k130_provenance.