Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_assertion wasGeneratedBy ECO_0000203 NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_assertion wasDerivedFrom befree-20150227 NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_assertion SIO_000772 20157192 NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_assertion evidence source_evidence_literature NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.
- NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_assertion description "[We also found a novel NKX2-1 variation (p.H60W) in a sporadic nonsyndromic CH patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739357.RADjSRwwwgZ-IUhwtye66mnRPclWViUzhvNnm4EMFvdE4130_provenance.