Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion> ?p ?o ?g. }
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- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion type Assertion NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_head.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion description "[Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion evidence source_evidence_literature NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion SIO_000772 16542388 NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion wasDerivedFrom gad-20150221 NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion wasGeneratedBy ECO_0000203 NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.