Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_assertion description "[Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_assertion evidence source_evidence_literature NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_assertion SIO_000772 16715098 NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_assertion wasDerivedFrom befree-2016 NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_assertion wasGeneratedBy ECO_0000203 NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.
- befree-2016 importedOn "2016-02-19" NP550784.RArtKWfgwliQj8yTzzjNhx0we55dv3TOn3fUVzov2gBDU130_provenance.