Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_assertion description "[Although mutations of the corresponding genes are rare events in SFT, PDGFR-alpha/beta, and hepatocyte growth factor receptor tyrosine kinases should be further investigated given the availability of specific inhibitory molecules which might provide useful and novel therapeutical approaches for SFT patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_assertion evidence source_evidence_literature NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_assertion SIO_000772 18753943 NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_assertion wasDerivedFrom befree-20140225 NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_assertion wasGeneratedBy ECO_0000203 NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP439477.RApettZns_00TTY_N_-xUmQWzjD7OxtEzRp6qzlqf4ojk130_provenance.