Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- befree-2016 importedOn "2016-02-19" NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_assertion wasGeneratedBy ECO_0000203 NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_assertion wasDerivedFrom befree-2016 NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_assertion SIO_000772 20578134 NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_assertion evidence source_evidence_literature NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.
- NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_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." NP821396.RA_nS1AZrJVIW62nZaSYo3bdoLofMpkgXsyV0oKh5X3ow130_provenance.