Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_assertion> ?p ?o ?g. }
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- NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_assertion type Assertion NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_head.
- NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_assertion wasGeneratedBy ECO_0000203 NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_provenance.
- NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_assertion wasDerivedFrom gad-20130706 NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_provenance.
- NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_assertion SIO_000772 19349604 NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_provenance.
- NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_assertion evidence source_evidence_literature NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_provenance.
- NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_assertion description "[In addition to mutation type and degree of X-chromosome skewing, the common brain-derived neurotrophic factor (BDNF) polymorphism appears to be another genetic modifier of Rett syndrome (RTT) severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82061.RAFbEO3A1Sc7OW4X9_-CcFkVndk17TkFNsOS9zGU9DSlY130_provenance.