Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_assertion description "[Three patients showed extra copies of chromosome 21 including a case in which the trisomy 21 (+21) clone was distinct from the one harboring TEL/AML1 gene fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_assertion evidence source_evidence_literature NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_assertion SIO_000772 11516105 NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_assertion wasDerivedFrom befree-2016 NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_assertion wasGeneratedBy ECO_0000203 NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.
- befree-2016 importedOn "2016-02-19" NP327745.RAD5b_rP2vMRN40SM-4kXpjTiYz1AyNCxq_yldW5piP-c130_provenance.