Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_assertion> ?p ?o ?g. }
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- NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_assertion type Assertion NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_head.
- NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_assertion description "[We conclude that the 5q-syndrome may be best defined as primary MDS of the FAB type RA with a 5q deletion as the sole karyotypic abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_provenance.
- NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_assertion evidence source_evidence_literature NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_provenance.
- NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_assertion SIO_000772 7604812 NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_provenance.
- NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_assertion wasDerivedFrom befree-20150227 NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_provenance.
- NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_assertion wasGeneratedBy ECO_0000203 NP606140.RAPHA_FE80VzPIJoQ9I6WPU6AZTIFRyJcxsOHe0c-jySA130_provenance.