Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_assertion description "[The glial cell missing gene, GCMB, encodes a transcription factor, which is a master regulator of parathyroid development/expression is upregulated in abnormal parathyroid glands of hyperparathyroidism and decreases in response to hypocalcemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_assertion evidence source_evidence_literature NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_assertion SIO_000772 15657585 NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_assertion wasDerivedFrom lhgdn-20090331 NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_assertion wasGeneratedBy ECO_0000203 NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.