Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_assertion description "[We report a novel congenital cataract causing mutation c.1751C>T in the EPHA2 gene and the previously reported splice mutation c.2826-9G>A in two new families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_assertion evidence source_evidence_literature NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_assertion SIO_000772 24014202 NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_assertion wasDerivedFrom befree-20150227 NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_assertion wasGeneratedBy ECO_0000203 NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP371636.RAtTFDM7VTGRcKlU_4adNAzuOpkel1VrZ9haRmajyznSw130_provenance.