Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion description "[A patient with episodic ataxia, seizures, migraine, and alternating hemiplegia has a heterozygous mutation in SLC1A3 that is not present in his asymptomatic parents and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion evidence source_evidence_literature NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion SIO_000772 16116111 NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion wasDerivedFrom befree-20140225 NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion wasGeneratedBy ECO_0000203 NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.