Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_assertion description "[A novel 8.5 MB dup(1)(p34.1p34.3) characterized by FISH in a child presenting with congenital heart defect and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_assertion evidence source_evidence_literature NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_assertion SIO_000772 16892326 NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_assertion wasDerivedFrom befree-20140225 NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_assertion wasGeneratedBy ECO_0000203 NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP408926.RAfRT89IxjZYAS8yG_zMjssYojVIjizlXkWffrNbPeo0g130_provenance.