Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_assertion> ?p ?o ?g. }
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- NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_assertion type Assertion NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_head.
- NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_assertion description "[The probability of finding FLNA mutations in other phenotypes was 4% but was limited to the minor variants of PNH with EDS and unilateral PNH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.
- NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_assertion evidence source_evidence_literature NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.
- NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_assertion SIO_000772 16684786 NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.
- NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_assertion wasDerivedFrom befree-20140225 NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.
- NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_assertion wasGeneratedBy ECO_0000203 NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.