Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_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." NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion evidence source_evidence_literature NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion SIO_000772 19247433 NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion wasDerivedFrom befree-2016 NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion wasGeneratedBy ECO_0000203 NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.
- befree-2016 importedOn "2016-02-19" NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.