Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_assertion description "[Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_assertion evidence source_evidence_literature NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_assertion SIO_000772 19838196 NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_assertion wasDerivedFrom befree-20140225 NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_assertion wasGeneratedBy ECO_0000203 NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP372875.RAGV_NcrOUHdvFQ95uvhU6iCn7LeH1cq2CI01GX2_Wddk130_provenance.