Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_assertion> ?p ?o ?g. }
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- NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_assertion type Assertion NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_head.
- NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_assertion description "[Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.
- NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_assertion evidence source_evidence_literature NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.
- NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_assertion SIO_000772 7536393 NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.
- NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_assertion wasDerivedFrom befree-20150227 NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.
- NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_assertion wasGeneratedBy ECO_0000203 NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.