Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_assertion type Assertion NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_head.
- NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_assertion description "[PITX2 mutations are known to be responsible for Axenfield Rieger syndrome, a genetic disorder in which pituitary abnormalities have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_provenance.
- NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_assertion evidence source_evidence_literature NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_provenance.
- NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_assertion SIO_000772 21810944 NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_provenance.
- NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_assertion wasDerivedFrom befree-20150227 NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_provenance.
- NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_assertion wasGeneratedBy ECO_0000203 NP626414.RAFkZv3ygtkctuz6Ryl2-pOEPXaWeTUtnnKbRhFHmGRKs130_provenance.