Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_assertion wasGeneratedBy ECO_0000203 NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_assertion wasDerivedFrom lhgdn-20090331 NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_assertion SIO_000772 18989701 NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_assertion evidence source_evidence_literature NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.
- NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_assertion description "[a gradient of impairment is present when the p.P152A mutation is compared with an allelic p.P152R mutation, which causes classic Rett syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243467.RA8G8nB_u369Xhk1hMPTtyG9IelqjY_QnmGplEhzMHg_A130_provenance.