Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_assertion description "[Mutations in PAX6 gene have been shown to be the genetic cause of aniridia, which is a severe panocular eye disease characterised by iris hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_assertion evidence source_evidence_literature NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_assertion SIO_000772 15740668 NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_assertion wasDerivedFrom befree-20140225 NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_assertion wasGeneratedBy ECO_0000203 NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430036.RA2F4eocbe69-dHGvqpD_Nts2PdiqKLI9ANWFAV2neEE4130_provenance.