Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_assertion type Assertion NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_head.
- NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_assertion wasGeneratedBy ECO_0000203 NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_provenance.
- NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_assertion wasDerivedFrom befree-2016 NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_provenance.
- NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_assertion SIO_000772 20164288 NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_provenance.
- NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_assertion evidence source_evidence_literature NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_provenance.
- NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_assertion description "[With a hypercalcemic family member, mutation detection rate in FHH rose to seven of eight (87%), whereas only one of nine sporadic cases was positive, and none of the three FIHP cases had detectable CASR mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794459.RA9ieVnWGhczCjMFwkex9Yh_bvo6iLHgdX-TH4zXc9sp0130_provenance.