Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_assertion description "[Inactivating HRPT2 mutations are common in HPT- JT and parathyroid carcinomas, and have been described in a few cases of parathyroid adenomas with cystic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_assertion evidence source_evidence_literature NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_assertion SIO_000772 16728578 NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_assertion wasDerivedFrom befree-20140225 NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_assertion wasGeneratedBy ECO_0000203 NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP324642.RAN8wI7AOh3gR0VyeRJC0boojmHyQuq2d3s8xSSqmZLsw130_provenance.