Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_assertion description "[In addition, no pathogenic sequence variations were found in DCN, DSPG3, LUM, PITX2 and FOXC1, which have also been implicated in corneal and anterior segment dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_assertion evidence source_evidence_literature NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_assertion SIO_000772 17558846 NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_assertion wasDerivedFrom befree-20140225 NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_assertion wasGeneratedBy ECO_0000203 NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP694773.RAPDnMfkrSRbG20aEenee05AC1gNPL-a4Y-e2dSKoIBv4130_provenance.