Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_assertion description "[A characteristic SYT-SSX fusion gene resulting from the chromosomal translocation t(X;18)(p11;q11) is detectable in almost all synovial sarcomas, a malignant soft tissue tumor widely believed to originate from as yet unidentified pluripotent stem cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_assertion evidence source_evidence_literature NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_assertion SIO_000772 19936258 NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_assertion wasDerivedFrom befree-20140225 NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_assertion wasGeneratedBy ECO_0000203 NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP386354.RAqbUVphhSnhdaHFfkr6M4jgyORbyXctEAkpH8QUmHFiE130_provenance.