Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_assertion description "[CEDNIK (cerebral dysgenesis, neuropathy, ichthyosis and keratoderma) syndrome is a rare genodermatosis which was shown 5 years ago in one family to be associated with a loss-of-function mutation in SNAP29, encoding a member of the SNARE family of proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_assertion evidence source_evidence_literature NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_assertion SIO_000772 21073448 NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_assertion wasDerivedFrom befree-2016 NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_assertion wasGeneratedBy ECO_0000203 NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP852171.RAeXlIVcOatBcBeeShQsJP5Avn5El41qD1tzaIaWT6yr4130_provenance.