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- source_evidence_literature type ECO_0000212 NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_assertion description "[Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_assertion evidence source_evidence_literature NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_assertion SIO_000772 9486973 NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_assertion wasDerivedFrom befree-2016 NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_assertion wasGeneratedBy ECO_0000203 NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.
- befree-2016 importedOn "2016-02-19" NP1389747.RArtFdqpZ0YDd_aiYd6MyulroNWah8DXJ7Mba44j_K8ns130_provenance.