Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_assertion wasGeneratedBy ECO_0000203 NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_assertion wasDerivedFrom befree-20140225 NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_assertion SIO_000772 18303074 NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_assertion evidence source_evidence_literature NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_assertion description "[The affected probands presented a similar phenotype characterized by a moderate postnatal growth deficit associated with undetectable ALS, low IGF-I, IGF-II, and IGFBP-3, and hyperinsulinemia, and, in two cases, delayed puberty.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563091.RAU-D6ZZbNscZhD2g1oV6YGVJ9O7rGh62GcNzp9GXb1qo130_provenance.