Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_assertion description "[The DNMT3A -448A>G polymorphism is a novel functional SNP and contributes to its genetic susceptibility to GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_assertion evidence source_evidence_literature NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_assertion SIO_000772 20128888 NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_assertion wasDerivedFrom befree-20150227 NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_assertion wasGeneratedBy ECO_0000203 NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP357806.RADGCG9XO2KHohyytbuZwaiWYMjw4PVe2qPs0sVAmq92s130_provenance.