Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP233662.RAwoVfyLpa_MB8k4xI8jc7YAUB8iIb_cTxR0SZ8cBTJAw130_provenance.