Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_assertion> ?p ?o ?g. }
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- NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_assertion type Assertion NP210526.RARMkh0v6daTlCfdTFPc_TCx4b5A6pgQLb47E8mvWC9Ug130_head.
- 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.