Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_assertion description "[Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_assertion evidence source_evidence_literature NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_assertion SIO_000772 17047887 NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_assertion wasDerivedFrom befree-20140225 NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_assertion wasGeneratedBy ECO_0000203 NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP175685.RA0C4lW56_eNUoSQrm_hRzVIPhNPWpLVJgOlTBGJ3TVqo130_provenance.