Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_assertion evidence source_evidence_literature NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_assertion SIO_000772 15174025 NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_assertion wasDerivedFrom befree-2016 NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_assertion wasGeneratedBy ECO_0000203 NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- befree-2016 importedOn "2016-02-19" NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.