Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_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." NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_assertion evidence source_evidence_literature NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_assertion SIO_000772 10051017 NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_assertion wasDerivedFrom befree-20150227 NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_assertion wasGeneratedBy ECO_0000203 NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP850338.RAnAdpxI7vOjy7FIOsuUM7503JgpZnX7WQ0D5dnwMEeGo130_provenance.