Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_assertion wasGeneratedBy ECO_0000203 NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_assertion wasDerivedFrom befree-20150227 NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_assertion SIO_000772 24048166 NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_assertion evidence source_evidence_literature NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.
- NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_assertion description "[Of note, additional patients who underwent a similar evaluation at our center for suspected GGM did not show mutations in the SLC5A1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697382.RAPtn1kH2d5q9Z76-DxCgao2DgR9onnVDgyaBz7NXo_uM130_provenance.