Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion> ?p ?o ?g. }
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- NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion type Assertion NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_head.
- NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_provenance.
- NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion evidence source_evidence_literature NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_provenance.
- NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion SIO_000772 17525745 NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_provenance.
- NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion wasDerivedFrom befree-2016 NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_provenance.
- NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion wasGeneratedBy ECO_0000203 NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_provenance.