Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_assertion description "[Here we have analyzed a balanced t(11;16)(p15;q13) chromosomal translocation associated with the BWS phenotype and mapped the breakpoint positions for both chromosomes 11 and 16 by using somatic cell hybrids and polymorphic markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_assertion evidence source_evidence_literature NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_assertion SIO_000772 7534105 NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_assertion wasDerivedFrom befree-20140225 NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_assertion wasGeneratedBy ECO_0000203 NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP546630.RAihmdYP5lWFgSjYKXLKSiXQw9PsbYkvlNJMZ-6_pYhMY130_provenance.