Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_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." NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_assertion evidence source_evidence_literature NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_assertion SIO_000772 17558846 NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_assertion wasDerivedFrom befree-20150227 NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_assertion wasGeneratedBy ECO_0000203 NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626419.RASMtl1WPZdofWPPXsq4HSgESmzB1u9J9i_NGBNa-ai38130_provenance.