Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- befree-2016 importedOn "2016-02-19" NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion wasGeneratedBy ECO_0000203 NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion wasDerivedFrom befree-2016 NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion SIO_000772 18627422 NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion evidence source_evidence_literature NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion description "[Mutation in PAX3 causes Waardenburg syndrome, and craniofacial-deafness-hand syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.