Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_assertion description "[We report a familial recombination of a pericentric inversion of chromosome 10 resulting in 2 affected relatives who had 10p trisomy and 10q monosomy with the karyotypic abnormality designated rec(10) dup p,inv(10) (p11.2q26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_assertion evidence source_evidence_literature NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_assertion SIO_000772 8209887 NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_assertion wasDerivedFrom befree-20140225 NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_assertion wasGeneratedBy ECO_0000203 NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP281287.RAmAH3tD4SHEUEJuHvumiy2zAZoaOU53nCcVugI25apRE130_provenance.