Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_assertion description "[Glycogen storage disease type IIIa (GSD IIIa) is an autosomal recessive disorder characterized by excessive accumulation of abnormal glycogen in the liver and muscles and caused by a deficiency in the glycogen debranching enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_assertion evidence source_evidence_literature NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_assertion SIO_000772 16189622 NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_assertion wasDerivedFrom befree-20140225 NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_assertion wasGeneratedBy ECO_0000203 NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583157.RAlHQCKGtFYldgbUfyIopTrPi1TmK_bXziyhVpl5rpa6o130_provenance.