Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_assertion evidence source_evidence_literature NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_assertion SIO_000772 21139041 NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_assertion wasDerivedFrom befree-20150227 NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_assertion wasGeneratedBy ECO_0000203 NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.