Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_assertion wasGeneratedBy ECO_0000203 NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_assertion wasDerivedFrom befree-20140225 NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_assertion SIO_000772 10396361 NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_assertion evidence source_evidence_literature NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_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." NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP182776.RAOHgM-Rj5xXBL8sd6wFTEIOHpQHrc3yE8OB9mvUaZebI130_provenance.