Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion description "[Our results suggest that characteristic sequence motifs located at the FUS, EWS and CHOP breakpoint regions, including Alu and palindromic oligomer sequences, are involved in the mechanisms creating chromosomal translocations in MLS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion evidence source_evidence_literature NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion SIO_000772 18752119 NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion wasDerivedFrom befree-20150227 NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion wasGeneratedBy ECO_0000203 NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance.