Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_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." NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_assertion evidence source_evidence_literature NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_assertion SIO_000772 20424473 NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_assertion wasDerivedFrom gad-20150221 NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_assertion wasGeneratedBy ECO_0000203 NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP127830.RAOm0Q0z0zkc5DaaEBoJIqGyDKSRvFX5w1dX_vHG7p-f4130_provenance.