Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_assertion wasGeneratedBy ECO_0000203 NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_assertion wasDerivedFrom befree-20140225 NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_assertion SIO_000772 16060937 NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_assertion evidence source_evidence_literature NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_assertion description "[Choreoacanthocytosis (ChAc) is an autosomal recessive disorder caused by mutations in VPS13A on chromosome 9q21 and characterized by neurodegeneration and red cell acanthocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.
- befree-20140225 importedOn "2014-02-25" NP892556.RAdYZtrvmFZ1_afMJy4k3TGjgsqtt80nrUn36ZVu-BQig130_provenance.