Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_assertion description "[Mutations within the RIEG1 homeobox gene on chromosome 4q25 have previously been reported in association with Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_assertion evidence source_evidence_literature NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_assertion SIO_000772 10051017 NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_assertion wasDerivedFrom befree-2016 NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_assertion wasGeneratedBy ECO_0000203 NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.
- befree-2016 importedOn "2016-02-19" NP246723.RAzEZ8zTCSBS0oa5iLGZa8Qk8uDDwMBJp2Lvf0FueNEJY130_provenance.