Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_assertion description "[Inherited defects that reduce the concentration of BH4, therefore, in general, lead to phenylketonuria and to deficiencies of dopamine and serotonin, as tyrosine hydroxylase and tryptophan hydroxylase are the rate-limiting enzymes required for the synthesis of these neurotransmitters.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_assertion evidence source_evidence_literature NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_assertion SIO_000772 17513427 NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_assertion wasDerivedFrom befree-20140225 NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_assertion wasGeneratedBy ECO_0000203 NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.
- befree-20140225 importedOn "2014-02-25" NP445827.RAMPfIyniEJ572OAuEllReB1ZnHGVKoA3pXx6ojbqhEls130_provenance.