Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_assertion type Assertion NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_head.
- NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_assertion description "[Cases with familial monosomy 7 are well recognized, but there are no reports of familial MDS with deletion of 5q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_provenance.
- NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_assertion evidence source_evidence_literature NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_provenance.
- NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_assertion SIO_000772 8217806 NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_provenance.
- NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_assertion wasDerivedFrom befree-20150227 NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_provenance.
- NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_assertion wasGeneratedBy ECO_0000203 NP605978.RAwkB3OVdbGgPJaDx2XCt7jhDlbne77GcSsZRGduz3rjk130_provenance.