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- source_evidence_literature type ECO_0000212 NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP147392.RAZzr5brqy-UooaFLGkIdgzTyJhCURDozNeK13LRSKexI130_provenance.