Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_assertion description "[By array comparative genomic hybridization (array-CGH), we identified a small duplication at Xq28 in a large family with a severe form of MR associated with progressive spasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_assertion evidence source_evidence_literature NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_assertion SIO_000772 16080119 NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_assertion wasDerivedFrom befree-20140225 NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_assertion wasGeneratedBy ECO_0000203 NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717899.RAk3NsIf0kHmocACUBXhHx1P6SaWuJmex0oVDAGS_8JW8130_provenance.