Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_assertion description "[A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_assertion evidence source_evidence_literature NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_assertion SIO_000772 15800843 NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_assertion wasDerivedFrom befree-2016 NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_assertion wasGeneratedBy ECO_0000203 NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.
- befree-2016 importedOn "2016-02-19" NP487793.RAqM73n8nAypPkv9LUnYmGuiM5Q8Mp1im-hg5xVY3lTaU130_provenance.