Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_assertion description "[In addition, haplotype analysis identified the gene for the alpha 1C subunit of the voltage-dependent L-type calcium channel (CACNA1C) as having a significant association with secondary hyperparathyroidism (intact parathyroid hormone level >200 pg/ml) among 61 haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_assertion evidence source_evidence_literature NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_assertion SIO_000772 20424473 NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_assertion wasDerivedFrom befree-20140225 NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_assertion wasGeneratedBy ECO_0000203 NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP269156.RA5VWfBakEU3hFsY4meHPZwfd7vf2-VJy0CXOtYXfMicw130_provenance.