Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_assertion evidence source_evidence_literature NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_assertion SIO_000772 8990006 NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_assertion wasDerivedFrom befree-20140225 NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_assertion wasGeneratedBy ECO_0000203 NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.