Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_assertion evidence source_evidence_literature NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_assertion SIO_000772 22893440 NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_assertion wasDerivedFrom befree-20140225 NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_assertion wasGeneratedBy ECO_0000203 NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.