Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_assertion description "[In contingent screening, a detection rate of 98% for trisomy 21 and 96% for trisomy 18 or 13, at an invasive testing rate of 0.7%, can be achieved by carrying out cfDNA testing in about 35, 20 and 11% of cases identified by first-line screening with the combined test alone (age, NT, FHR, ?-hCG, PAPP-A), the combined test plus PLGF and AFP and the combined test plus PLGF, AFP and DV PIV, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_assertion evidence source_evidence_literature NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_assertion SIO_000772 24192489 NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_assertion wasDerivedFrom befree-2016 NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_assertion wasGeneratedBy ECO_0000203 NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1125140.RAXoUTxrdZKPJbszgbiIkG6FbLEBG6fl19BsI72Unvfbw130_provenance.