Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_assertion description "[X-linked lissencephaly with corpus callosum agenesis and ambiguous genitalia in genotypic males is associated with mutations of the ARX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_assertion evidence source_evidence_literature NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_assertion SIO_000772 16724181 NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_assertion wasDerivedFrom befree-2016 NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_assertion wasGeneratedBy ECO_0000203 NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP551518.RA6Ulmyjbn3zeis0w17Dr3kT3lA00YPDapGi41f4ConVQ130_provenance.