Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- befree-2016 importedOn "2016-02-19" NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_assertion wasGeneratedBy ECO_0000203 NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_assertion wasDerivedFrom befree-2016 NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_assertion SIO_000772 19251738 NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_assertion evidence source_evidence_literature NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_assertion description "[These features are similar to those of gene enhancer elements, raising the possibility that CHD7 functions in enhancer mediated transcription, and that the congenital anomalies in CHARGE syndrome are due to alterations in transcription of tissue-specific genes normally regulated by CHD7 during development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.