Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_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." NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion evidence source_evidence_literature NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion SIO_000772 19698724 NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion wasDerivedFrom befree-2016 NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion wasGeneratedBy ECO_0000203 NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.
- befree-2016 importedOn "2016-02-19" NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance.