Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_assertion description "[Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_assertion evidence source_evidence_literature NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_assertion SIO_000772 23830518 NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_assertion wasDerivedFrom befree-2016 NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_assertion wasGeneratedBy ECO_0000203 NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1091758.RAxJC2QLN61arZInZGVcwz7Mq12vHCJZou78iDr_KSEiU130_provenance.