Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_assertion description "[To determine the incidence, natural history, and mechanism of C cell dysfunction in PHP, calcitonin assays were performed in six patients with PHP Ia and four with pseudopseudohypoparathyroidism from three unrelated families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_assertion evidence source_evidence_literature NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_assertion SIO_000772 11443172 NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_assertion wasDerivedFrom befree-20140225 NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_assertion wasGeneratedBy ECO_0000203 NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP644056.RADWfrsDkQTADn1TFKSgP8UipNXa2lSLbHaWx_RGzkvBs130_provenance.