Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_assertion description "[In this large series, HNF4A mutations are the third most common cause of diazoxide responsive HH. We recommend that HNF4A sequencing is considered in all patients with diazoxide responsive HH diagnosed in the first week of life irrespective of a family hi]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_assertion evidence source_evidence_literature NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_assertion SIO_000772 20164212 NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_assertion wasDerivedFrom gad-20150221 NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_assertion wasGeneratedBy ECO_0000203 NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.
- gad-20150221 importedOn "2015-02-21" NP138086.RAStUFV-p9WMMBxUmR4UeGyeU3a1dDI0DnTvjrPo6BQ8Y130_provenance.