Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_assertion wasGeneratedBy ECO_0000203 NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_assertion wasDerivedFrom befree-2016 NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_assertion SIO_000772 25146893 NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_assertion evidence source_evidence_literature NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.
- NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_assertion description "[Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1212720.RAMvPwKyK1lQyu9SArLouwA3UJQvX6GyfeTOw2HsNxpSA130_provenance.