Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- befree-2016 importedOn "2016-02-19" NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_assertion wasGeneratedBy ECO_0000203 NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_assertion wasDerivedFrom befree-2016 NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_assertion SIO_000772 11260864 NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_assertion evidence source_evidence_literature NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.
- NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_assertion description "[Based on the pattern of altered genes and their correlation with clinical and pathological parameters, the genetic alterations were classified into three groups: group I: no detectable genetic alterations (n = 3, 13.6%); group II: LOH in APC and/or DCC (n = 9, 40.9%); and group III: LOH in OGG1 and/or p53 occurred separately or combined with LOH in APC and/or DCC (n = 10, 45.5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311720.RABx7s_4kYbDbFFSth0zemxOoy_fn-i29NhNDh3NPeAq0130_provenance.