Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_assertion type Assertion NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_head.
- NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_assertion wasGeneratedBy ECO_0000203 NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_provenance.
- NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_assertion wasDerivedFrom lhgdn-20090331 NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_provenance.
- NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_assertion SIO_000772 18182452 NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_provenance.
- NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_assertion evidence source_evidence_literature NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_provenance.
- NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_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." NP233102.RA_HOT1Gq6YhXpeyTSpJ0-2agNEQ6dzbsBBjhRZvB5ySE130_provenance.