Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_assertion wasGeneratedBy ECO_0000218 NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_assertion wasDerivedFrom ctd_human-20130708 NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_assertion SIO_000772 17704776 NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_assertion evidence source_evidence_curated NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_assertion description "[Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP30839.RAGRlgjWjWcQqUEp81TFpiQiLHunBmRsoKHvgzccpjyh8130_provenance.