Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_assertion description "[Autosomal dominant hypocalcemia (ADH) is an inherited form of hypoparathyroidism caused by activating mutations in the calcium-sensing receptor (CaR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_assertion evidence source_evidence_literature NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_assertion SIO_000772 19063686 NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_assertion wasDerivedFrom befree-20140225 NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_assertion wasGeneratedBy ECO_0000203 NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP423968.RArgIegwa-5Pm4Xuw8HtgTeo5QcPW8RUPbGo4MW4S5wUY130_provenance.