Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_assertion wasGeneratedBy ECO_0000203 NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_assertion wasDerivedFrom befree-20140225 NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_assertion SIO_000772 8558938 NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_assertion evidence source_evidence_literature NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_assertion description "[Recurring aberrations, found in 76% of children, included t(15;17)(q22;q11), t(8;21)(q22;q22), inv(16)(p13q22), rearrangements of band 11q23, t(6;9) (p23;q34), trisomy 8 and monosomy 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP523728.RAo_-L4l7UXhz68li9S19gAQwj7fpdt5nqt-d1pXIKJng130_provenance.