Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_assertion description "[Autosomal dominant hypocalcemia (ADH) is an inherited form of hypoparathyroidism caused by activating mutations in the calcium-sensing receptor (CaR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_assertion evidence source_evidence_literature NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_assertion SIO_000772 19063686 NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_assertion wasDerivedFrom befree-2016 NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_assertion wasGeneratedBy ECO_0000203 NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.
- befree-2016 importedOn "2016-02-19" NP707752.RAom_r9i0YqoBv6FtbKO24mqosJATIuROoOYT3_FmUJec130_provenance.