Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion description "[Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion evidence source_evidence_literature NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion SIO_000772 19279310 NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion wasDerivedFrom befree-20150227 NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion wasGeneratedBy ECO_0000203 NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.