Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_assertion description "[This disease-causing mutation is a single basepair change (G to A) in the splice-acceptor region of APC intron 3 that creates a mutant RNA without exon 4 of APC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_assertion evidence source_evidence_literature NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_assertion SIO_000772 10598803 NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_assertion wasDerivedFrom befree-20140225 NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_assertion wasGeneratedBy ECO_0000203 NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_provenance.