Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285282.RARlaafElymSZ1_X1qLY_sJHrL9eKEVKivkW1-EWWr-Y4130_provenance.
- 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.