Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_assertion type Assertion NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_head.
- NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_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." NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_provenance.
- NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_assertion evidence source_evidence_literature NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_provenance.
- NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_assertion SIO_000772 7604812 NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_provenance.
- NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_assertion wasDerivedFrom befree-20150227 NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_provenance.
- NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_assertion wasGeneratedBy ECO_0000203 NP978675.RAH9-SpYZIOHlXj9wU7-M1q-f7ZFc1nkA31csgYUNrNtc130_provenance.