Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_assertion> ?p ?o ?g. }
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- NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_assertion type Assertion NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_head.
- NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_assertion wasGeneratedBy ECO_0000203 NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_provenance.
- NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_assertion wasDerivedFrom befree-20140225 NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_provenance.
- NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_assertion SIO_000772 11106355 NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_provenance.
- NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_assertion evidence source_evidence_literature NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_provenance.
- NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_assertion description "[The incidence of exomphalos in putative BWSIC2 defect patients was not significantly different from that in patients with germline CDKN1C mutations (20/29 and 13/15 respectively), but was significantly greater than that in patients with putative BWSIC1 defects (0/5, p=0.007) and UPD (0/22, p<0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843301.RAF6lVf6krEb-Vle4Pw1FG7seuePU6dkETDvO1x6ibq0A130_provenance.