Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_assertion description "[By using probes specific for the c-mos and c-myc genes, we have analysed the genomic DNA from peripheral blood and bone marrow samples from 15 patients with various malignant myeloid diseases, including leukemia and myelodysplasia, and from one patient with non-Hodgkin's lymphoma, all of whom have trisomy for chromosome No.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_assertion evidence source_evidence_literature NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_assertion SIO_000772 4079453 NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_assertion wasDerivedFrom befree-20150227 NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_assertion wasGeneratedBy ECO_0000203 NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP581427.RAzF6mpV0KYh7wXh4euohPQUO6ETg9xDwJRpp80g4NsLc130_provenance.