Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP819304.RANBMCZk7JLk1JRXdIzrkxtjI_7DXr3XnihH1TSuFZ51A130_provenance.