Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_assertion wasGeneratedBy ECO_0000203 NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_assertion wasDerivedFrom befree-20140225 NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_assertion SIO_000772 18726931 NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_assertion evidence source_evidence_literature NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_assertion description "[Genomic rearrangements comprising both deletions encompassing FOXL2 and deletions located outside its transcription unit, represent 12% and 5% of all genetic defects in our BPES cohort, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP210284.RAtB-D3KtYecOKVdgsIU4yWoIM4sxw38A4Zd6UpIJrxmI130_provenance.