Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_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." NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_assertion evidence source_evidence_literature NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_assertion SIO_000772 15657585 NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_assertion wasDerivedFrom lhgdn-20090331 NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_assertion wasGeneratedBy ECO_0000203 NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP208800.RAyoQlIz21434tAdvi6JOCB6SJ92pENXKdJvSLa4oWYao130_provenance.