Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_assertion> ?p ?o ?g. }
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- NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_assertion type Assertion NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_head.
- NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_assertion description "[The common aberration found in these two t-MDS cases was the fragility of chromosome 5 and monosomy of chromosome 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_provenance.
- NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_assertion evidence source_evidence_literature NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_provenance.
- NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_assertion SIO_000772 12505257 NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_provenance.
- NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_assertion wasDerivedFrom befree-2016 NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_provenance.
- NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_assertion wasGeneratedBy ECO_0000203 NP378941.RANKogQpmKQFv-hKbF425gewadtRYANHFOAKrjtdLhYDg130_provenance.