Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_assertion wasGeneratedBy ECO_0000203 NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_assertion wasDerivedFrom lhgdn-20090331 NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_assertion SIO_000772 18182452 NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_assertion evidence source_evidence_literature NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.
- NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_assertion description "[Although GCM2 mutations appear to be an uncommon cause of isolated hypoparathyroidism, the wide variety of GCM2 polymorphisms suggests that variant alleles may have a role in determining parathyroid function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_provenance.