Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_assertion description "[This study was designed to define the prevalence of CH due to mutations of PAX8, NKX2-1 [encoding thyroid transcription factor (TTF)-1], FOXE1 (encoding TTF-2), and NKX2-5 among patients with permanent primary CH and in the general population in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_assertion evidence source_evidence_literature NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_assertion SIO_000772 20157192 NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_assertion wasDerivedFrom befree-20140225 NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_assertion wasGeneratedBy ECO_0000203 NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380236.RAm9DKkJ8930zosvUon9T0KTPOLNqHLNsLC8yiNR9GJ8g130_provenance.