Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_assertion wasGeneratedBy ECO_0000203 NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_assertion wasDerivedFrom befree-20140225 NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_assertion SIO_000772 10396361 NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_assertion evidence source_evidence_literature NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_assertion description "[Familial hyperparathyroidism may occur as familial isolated hyperparathyroidism (FIHP) or as part of an inherited syndrome, in particular multiple endocrine neoplasia types 1 and 2A (MEN1, MEN2A) and hyperparathyroidism-jaw tumour (HPT-JT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP455925.RA9sAIt0dyXVOAZVON3Z8h9rGEKU0lgHMReZreAhn-MbA130_provenance.