Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_assertion description "[The distribution of CALM3 genotypes differed in 180 unrelated FHC patients carrying a known FHC mutation compared with 134 controls, with higher TT-genotype frequency (0.73 vs. 0.51) and lower frequencies of AT- (0.24 vs. 0.37) and AA genotypes (0.03 vs. 0.11; P = 0.0005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_assertion evidence source_evidence_literature NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_assertion SIO_000772 19429631 NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_assertion wasDerivedFrom befree-20140225 NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_assertion wasGeneratedBy ECO_0000203 NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP544791.RAKGkLpj7t0gfmPXfpc9wr-Vj7wU0U25lxX_BAt6z1tvg130_provenance.