Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_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." NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_assertion evidence source_evidence_literature NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_assertion SIO_000772 19247433 NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_assertion wasDerivedFrom befree-20140225 NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_assertion wasGeneratedBy ECO_0000203 NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.