Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_assertion> ?p ?o ?g. }
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- NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_assertion type Assertion NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_head.
- NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_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." NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_provenance.
- NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_assertion evidence source_evidence_literature NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_provenance.
- NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_assertion SIO_000772 21810944 NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_provenance.
- NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_assertion wasDerivedFrom befree-2016 NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_provenance.
- NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_assertion wasGeneratedBy ECO_0000203 NP914257.RAtoccisMSprh3YGofkbywauKVvdj3mP7psRHJkd4uuWU130_provenance.