Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_assertion> ?p ?o ?g. }
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- NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_assertion type Assertion NP237655.RARumxUswVJHryWjkOlRoxi_AmdgXP8_OpFwyST9WjX5E130_head.
- 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.