Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_assertion description "[These results indicate that the SRJ domain is dispensable for these functions of CITED2 in mice and that mutations clustering in the SRJ region are unlikely to be the sole cause of the malformations observed in patients with sporadic CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_assertion evidence source_evidence_literature NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_assertion SIO_000772 23082118 NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_assertion wasDerivedFrom befree-2016 NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_assertion wasGeneratedBy ECO_0000203 NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1022470.RA9p3ZuiMLJzm_i8ZhJE4Ljw5Nwv8RKkyQLuNqU1GmKEY130_provenance.