Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_assertion wasGeneratedBy ECO_0000203 NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_assertion wasDerivedFrom befree-2016 NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_assertion SIO_000772 9748047 NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_assertion evidence source_evidence_literature NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.
- NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_assertion description "[A Chinese male infant with arthrogryposis multiplex congenita (AMC), ventricular and atrial septal defects, and Werdnig-Hoffmann disease (WHD) had deletions of the telomeric copy of the survival motor neuron (SMN(T)) and neuronal apoptosis inhibitory protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404516.RAa8Ih6jzVpfI2DnhBs0zJ4kM6yoleU_DafX2tBVgKgYM130_provenance.