Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_assertion> ?p ?o ?g. }
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- NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_assertion type Assertion NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_head.
- NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_assertion wasGeneratedBy ECO_0000203 NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.
- NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_assertion wasDerivedFrom lhgdn-20090331 NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.
- NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_assertion SIO_000772 18182452 NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.
- NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_assertion evidence source_evidence_literature NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.
- NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_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." NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.