Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_assertion description "[Usher type 1C maps to the region containing the genes ABCC8 and KCNJ11 (encoding components of ATP-sensitive K + (KATP) channels), which may be mutated in patients with hyperinsulinism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_assertion evidence source_evidence_literature NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_assertion SIO_000772 10973248 NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_assertion wasDerivedFrom befree-20140225 NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_assertion wasGeneratedBy ECO_0000203 NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP229469.RAF_tIWL-K4wJl_kiLmskE1IEAx57aBc550sQwLrvK4bU130_provenance.