Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_assertion description "[The proband was a male with Ohtahara syndrome, ambiguous genitalia, psychomotor delay, and central nervous system dysgenesis due to a novel ARX mutation in exon 5, causing a frameshift in the aristaless domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_assertion evidence source_evidence_literature NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_assertion SIO_000772 21426321 NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_assertion wasDerivedFrom befree-2016 NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_assertion wasGeneratedBy ECO_0000203 NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP881489.RAlavBfs4GhsihPqbFEGP1QzL1cP4gNTgGdF9s_GdUdJQ130_provenance.