Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_assertion evidence source_evidence_literature NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_assertion SIO_000772 20424473 NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_assertion wasDerivedFrom gad-20130706 NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_assertion wasGeneratedBy ECO_0000203 NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP86246.RAl-nrLj_XCvtwqOXu2-l4snKLcQ6rjpNt3Rmwo6nJqrg130_provenance.