Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_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." NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_assertion evidence source_evidence_literature NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_assertion SIO_000772 20424473 NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_assertion wasDerivedFrom befree-2016 NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_assertion wasGeneratedBy ECO_0000203 NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.
- befree-2016 importedOn "2016-02-19" NP808690.RAXbYnHlDPX2vSoRQ84xP1W8fZksgCUs__BmJAa0pRmEI130_provenance.