Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_assertion description "[Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_assertion evidence source_evidence_literature NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_assertion SIO_000772 15565467 NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_assertion wasDerivedFrom befree-2016 NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_assertion wasGeneratedBy ECO_0000203 NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.
- befree-2016 importedOn "2016-02-19" NP470367.RAIfUz7OwYrYYmY745L1FmS7pvpKn09YkDh-ER0x_t_mM130_provenance.