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- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion type Assertion NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_head.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion description "[We describe prenatal genetic testing of FGFR2 in a fetus of a mother whose previous child had Crouzon Syndrome due to an apparently de novo mutation, S351C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion evidence source_evidence_literature NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion SIO_000772 15916101 NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion wasDerivedFrom befree-20140225 NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion wasGeneratedBy ECO_0000203 NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.