Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_assertion description "[Previously, we studied mutations of the FANCA gene, responsible for FA-A, and found pathogenic mutations in 12 of 15 unclassified Japanese FA patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_assertion evidence source_evidence_literature NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_assertion SIO_000772 10807541 NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_assertion wasDerivedFrom befree-2016 NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_assertion wasGeneratedBy ECO_0000203 NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.
- befree-2016 importedOn "2016-02-19" NP283588.RA4f2JICVyBj0NAMQeDr4jY9gJvZ1ux9xQTnNNKuzsDvE130_provenance.