Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_assertion description "[Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_assertion evidence source_evidence_literature NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_assertion SIO_000772 12139752 NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_assertion wasDerivedFrom gad-20130706 NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_assertion wasGeneratedBy ECO_0000203 NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP50510.RAKJ9UNCr0_l8cZp5PUuzAq4kyNlG_NjLmcW4lxLE8IpQ130_provenance.