Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP752001.RAqSHGI3voS0GH1dEIfmfWDG7s2E81y4P_nqLB2APRtdw130_provenance.