Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion description "[We assessed a family in which the translocation between chromosomes 12 and 16 segregates; one of the eight progenies with the karyotype 47,XY,+21,t(12;16)(q24;q24) was heterozygote for the translocation and presented with Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion evidence source_evidence_literature NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion SIO_000772 18990986 NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion wasDerivedFrom befree-20140225 NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion wasGeneratedBy ECO_0000203 NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.