Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_assertion description "[However, the function of GPR56 remained unclear until 2004 when mutations in the human GPR56 gene were found to cause a specific brain malformation called bilateral frontoparietal polymicrogyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_assertion evidence source_evidence_literature NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_assertion SIO_000772 20374731 NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_assertion wasDerivedFrom befree-20150227 NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_assertion wasGeneratedBy ECO_0000203 NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP819638.RApAvD9EaOLhAQA28CJThf3NO4jwWg9hWBxgFUPC0mqZg130_provenance.