Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_assertion description "[In conclusion, mutations of GABRA1, GABRB3, and GABRG2 appear not to play a major role in the development of familial primary dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_assertion evidence source_evidence_literature NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_assertion SIO_000772 17880575 NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_assertion wasDerivedFrom befree-20140225 NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_assertion wasGeneratedBy ECO_0000203 NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.
- befree-20140225 importedOn "2014-02-25" NP906108.RAY2RmGh2JMLdwIQfjKjNsNpuQwQ0smCfpGqrpDT_urho130_provenance.