Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_assertion type Assertion NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_head.
- NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_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." NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_provenance.
- NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_assertion evidence source_evidence_literature NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_provenance.
- NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_assertion SIO_000772 7604812 NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_provenance.
- NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_assertion wasDerivedFrom befree-20140225 NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_provenance.
- NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_assertion wasGeneratedBy ECO_0000203 NP193132.RA-G7W8hol9RzOKflboHqVyEQ01rPaU3Fm_2c1HMmidns130_provenance.