Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_assertion> ?p ?o ?g. }
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- NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_assertion type Assertion NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_head.
- NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_assertion wasGeneratedBy ECO_0000203 NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_assertion wasDerivedFrom befree-20150227 NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_assertion SIO_000772 20578134 NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_assertion evidence source_evidence_literature NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_assertion description "[Comparing the clinical features of our patients with the overlapping ones already reported two potential phenotypes related to 21q22 microdeletion including RUNX1 were highlighted: thrombocytopenia with +/- mild dysmorphic features and syndromic thrombocytopenia with growth and developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.