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- source_evidence_literature type ECO_0000212 NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_assertion description "[In conclusion HF1 mutations are frequent in patients with D-HUS (24%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_assertion evidence source_evidence_literature NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_assertion SIO_000772 14583443 NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_assertion wasDerivedFrom befree-20140225 NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_assertion wasGeneratedBy ECO_0000203 NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP602630.RAgdWzS0orNjsF-9fGuvzVJ8SOvUQNwiQ6xkfOeqiJBH8130_provenance.