Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_assertion description "[Autosomal dominant hypocalcemia (ADH) caused by activating mutations of calcium-sensing receptor (CaSR) is characterized by hypocalcemia with inappropriately low concentration of PTH and relative hypercalciuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_assertion evidence source_evidence_literature NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_assertion SIO_000772 12733714 NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_assertion wasDerivedFrom befree-20140225 NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_assertion wasGeneratedBy ECO_0000203 NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212064.RAcdfyFY35c_KiP5dctix-w4CMlKGT8FvLVG3V8kLEm-4130_provenance.