Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_assertion evidence source_evidence_literature NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_assertion SIO_000772 9932941 NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_assertion wasDerivedFrom befree-2016 NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_assertion wasGeneratedBy ECO_0000203 NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.