Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_assertion> ?p ?o ?g. }
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- NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_assertion type Assertion NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_head.
- NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_assertion description "[In addition, the infant had some features reminiscent of Beckwith Wiedemann syndrome including macroglossia, umbilical hernia, and a relatively large birth weight and we speculate that this is due to the deletion of GRB10, an imprinted gene on chromosome 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.
- NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_assertion evidence source_evidence_literature NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.
- NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_assertion SIO_000772 20933618 NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.
- NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_assertion wasDerivedFrom befree-20140225 NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.
- NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_assertion wasGeneratedBy ECO_0000203 NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.