Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP412779.RAX37Tvk2QquKTSuDExerPPSsdRAxozdXEoJt6zSEIWiM130_provenance.