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- source_evidence_literature type ECO_0000212 NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_assertion evidence source_evidence_literature NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_assertion SIO_000772 19247433 NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_assertion wasDerivedFrom befree-20150227 NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_assertion wasGeneratedBy ECO_0000203 NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.