Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_assertion description "[In conclusion, this case report of MEN 2A linked to a 634 RET mutation was peculiar by its revelation mode (1) hyperparathyroidism moreover linked to an adenoma and (2) associated with diabetes, mechanisms of which are probably multifactorial (familial type 2 diabetes, hypercalcemia, catecholamines excess).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_assertion evidence source_evidence_literature NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_assertion SIO_000772 18752792 NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_assertion wasDerivedFrom befree-2016 NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_assertion wasGeneratedBy ECO_0000203 NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.
- befree-2016 importedOn "2016-02-19" NP690103.RAi-Ro1UG0yx_Q0kxjQGDvBoDJNnD1Pm3OsePfg0ZRO6U130_provenance.