Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_assertion description "[As predicted by the APC germline mutations among these patients, a high percentage (29%) of FAP-associated desmoids showed loss of the APC region at 5q22.2, which was infrequently (3%) seen among sporadic tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_assertion evidence source_evidence_literature NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_assertion SIO_000772 21931686 NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_assertion wasDerivedFrom befree-2016 NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_assertion wasGeneratedBy ECO_0000203 NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.
- befree-2016 importedOn "2016-02-19" NP924926.RA4MW45mKKopU9Ww0H92nNykZkkYMkSdVqdMcpz_cQoFY130_provenance.