Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_assertion description "[Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation--a neurophysiological study using excitability techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_assertion evidence source_evidence_literature NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_assertion SIO_000772 22192498 NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_assertion wasDerivedFrom befree-20140225 NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_assertion wasGeneratedBy ECO_0000203 NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP622103.RAUC5oWkCTfyGXoqDp04N2jmd_jhbq_MuQcW90NiP4YKs130_provenance.