Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_assertion description "[To investigate catecholamine phenotypes and the effects of a tyrosine hydroxylase inhibitor in individuals with the 22q11.2 deletion syndrome and low-activity catechol-O-methyltransferase (COMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_assertion evidence source_evidence_literature NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_assertion SIO_000772 11502905 NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_assertion wasDerivedFrom befree-2016 NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_assertion wasGeneratedBy ECO_0000203 NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP327049.RAp97ZbBK3jAZF0DFeH_U6vq_yt0ZkbKSpOYMQ1gANZJ4130_provenance.