Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_assertion description "[In this study, we tested the hypothesis that mutations in the GABRA1, GABRB3, and GABRG2 genes encoding the alpha1, beta3, and gamma subunits of the GABA(A) receptor are involved in familial primary dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_assertion evidence source_evidence_literature NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_assertion SIO_000772 17880575 NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_assertion wasDerivedFrom befree-20140225 NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_assertion wasGeneratedBy ECO_0000203 NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718548.RAznzQBlU9SQIE1FGhl9DpPEuwnU5_ot2t3-IMSzpENFo130_provenance.