Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_assertion description "[We studied nine Italian families with a pure form of autosomal dominant spastic paraplegia (ADHSP) to assess the frequency of mutations in the SPG4 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_assertion evidence source_evidence_literature NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_assertion SIO_000772 11985387 NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_assertion wasDerivedFrom befree-20140225 NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_assertion wasGeneratedBy ECO_0000203 NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP781893.RA7_9eDu92WY8VFMpfOlKcPJqX9KoOnXKfwKvjpnqD1Bs130_provenance.