Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_assertion wasGeneratedBy ECO_0000203 NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_assertion wasDerivedFrom befree-20150227 NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_assertion SIO_000772 24664538 NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_assertion evidence source_evidence_literature NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.
- NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_assertion description "[Mutations in PAX5, and RUSC2, were seen exclusively in ALL patients and those in KIAA1432, CA9, TLN1, and MELK only in sarcomas (MFH, FS, EFT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610183.RA_t1mkoww3ihBmx0EjjOcgLfrmw7ZrS9JiSMdDLMHwpc130_provenance.