Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_assertion description "[Combining cytogenetic complexity and transcript data, we found that the subgroup of patients with tumors showing simple karyotypes and SYT/SSX2 fusion had the best clinical outcome (2/8 patients developed metastases), and those with tumors showing complex karyotypes together with SYT/SSX1 fusion the worst (6/7 patients developed metastases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_assertion evidence source_evidence_literature NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_assertion SIO_000772 11433527 NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_assertion wasDerivedFrom befree-20150227 NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_assertion wasGeneratedBy ECO_0000203 NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP714943.RALMM4tqP2ik8EMByFyFThK35GdEFajlwv6WXVS2Q38NE130_provenance.