Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_assertion description "[Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_assertion evidence source_evidence_literature NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_assertion SIO_000772 20094846 NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_assertion wasDerivedFrom gad-20150221 NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_assertion wasGeneratedBy ECO_0000203 NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP83668.RANl515CWM4_Zs1pfbhrDe5o8Uuqop_UxvQh4MTA5BCgc130_provenance.