Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- befree-2016 importedOn "2016-02-19" NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_assertion wasGeneratedBy ECO_0000203 NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_assertion wasDerivedFrom befree-2016 NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_assertion SIO_000772 20718765 NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_assertion evidence source_evidence_literature NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.
- NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_assertion description "[Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833507.RAqhJzfq3z9b21rovC7XA_x9Bsch0m9ZtiWWBv8wFoGDg130_provenance.