Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_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." NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_assertion evidence source_evidence_literature NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_assertion SIO_000772 17513427 NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_assertion wasDerivedFrom befree-2016 NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_assertion wasGeneratedBy ECO_0000203 NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.
- befree-2016 importedOn "2016-02-19" NP610859.RA7DP3MFQ9YVFZ9g3nBl9LTtf0ZCUPNKeELWcOX5O6FX8130_provenance.