Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_assertion type Assertion NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_head.
- NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_assertion wasGeneratedBy ECO_0000203 NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.
- NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_assertion wasDerivedFrom befree-20140225 NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.
- NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_assertion SIO_000772 20164288 NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.
- NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_assertion evidence source_evidence_literature NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.
- NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_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." NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.