Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_assertion description "[The autosomal dominantly inherited condition familial hypocalciuric hypercalcemia (FHH) is characterized by elevated plasma calcium levels, relative or absolute hypocalciuria, and normal to moderately elevated plasma PTH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_assertion evidence source_evidence_literature NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_assertion SIO_000772 17698911 NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_assertion wasDerivedFrom befree-20140225 NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_assertion wasGeneratedBy ECO_0000203 NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP680660.RAgmPh0ce8Szyeh6AgUtpCq62i14HfHMkdiq6JqWbCsxg130_provenance.