Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion description "[This study enables us to estimate the frequency of the SPG3A mutations in France at 39% in families with young-onset autosomal dominant spastic paraplegia after exclusion of SPG4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion evidence source_evidence_literature NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion SIO_000772 15596607 NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion wasDerivedFrom befree-20140225 NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion wasGeneratedBy ECO_0000203 NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.