Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_assertion description "[The progressive neurological abnormalities, congenital hypopituitarism and post-retinal visual pathway dysfunction in affected individuals demonstrates for the first time the essential role of ARNT2 in the development of the hypothalamo-pituitary axis, post-natal brain growth, and visual and renal function in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_assertion evidence source_evidence_literature NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_assertion SIO_000772 24022475 NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_assertion wasDerivedFrom befree-2016 NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_assertion wasGeneratedBy ECO_0000203 NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1109153.RAkhyAZ5x9j83L2uMlLGElJGa0lD-QK0inBghbqhumwTE130_provenance.