Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_assertion> ?p ?o ?g. }
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- NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_assertion type Assertion NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_head.
- NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_assertion description "[Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_provenance.
- NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_assertion evidence source_evidence_literature NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_provenance.
- NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_assertion SIO_000772 19066959 NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_provenance.
- NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_assertion wasDerivedFrom befree-20150227 NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_provenance.
- NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_assertion wasGeneratedBy ECO_0000203 NP401672.RARRyzYVVmXD43haVjmDVC2kH8r5dIRc2YHZCFy7lpVew130_provenance.