Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_assertion> ?p ?o ?g. }
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- NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_assertion type Assertion NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_head.
- NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_assertion description "[Identification of polymorphic sites within NET, specifically those that produce functional consequences, is one critical step in elucidating the genetic variation contributing to the heritable component of diseases such as ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_provenance.
- NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_assertion evidence source_evidence_literature NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_provenance.
- NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_assertion SIO_000772 19698724 NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_provenance.
- NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_assertion wasDerivedFrom befree-20150227 NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_provenance.
- NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_assertion wasGeneratedBy ECO_0000203 NP376342.RAIkwccwYwr59wXBsYaA2gYfHv9HeLmELS2YVNH3znZm4130_provenance.