Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_assertion description "[ARX is a crucial gene for the development of interneurons in the fetal brain, and a polyalanine expansion mutation of ARX causes mental retardation and seizures, including those of West syndrome, in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_assertion evidence source_evidence_literature NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_assertion SIO_000772 17668384 NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_assertion wasDerivedFrom befree-20140225 NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_assertion wasGeneratedBy ECO_0000203 NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624650.RALEj85Xj5WFTckCM426LOQTIgCys_Y7Q4zkF6_X_iKrw130_provenance.