Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_assertion wasGeneratedBy ECO_0000203 NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_assertion wasDerivedFrom befree-2016 NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_assertion SIO_000772 23771323 NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_assertion evidence source_evidence_literature NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.
- NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_assertion description "[Both classic FAP and attenuated FAP phenotypes were associated with BE .Two types of germ line mutations in APC gene were identified in BE(+)/FAP(+) patients: Five patients had 2-base deletion in exon 4 (426delAT) and one patient had 4-base deletion in exon 15 (3202del4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086336.RAA5I5g0yliGzdUBVO5JxnG86ScmXXQXllae8qlqp93xM130_provenance.