Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_assertion description "[Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_assertion evidence source_evidence_literature NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_assertion SIO_000772 16080119 NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_assertion wasDerivedFrom lhgdn-20090331 NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_assertion wasGeneratedBy ECO_0000203 NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP212286.RAQieqW4VRud9UJgWa6cGH4IlOsbpIPy5o5CwgerHNf8Q130_provenance.