Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_assertion description "[A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_assertion evidence source_evidence_literature NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_assertion SIO_000772 15249611 NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_assertion wasDerivedFrom befree-20140225 NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_assertion wasGeneratedBy ECO_0000203 NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP549742.RABpiOdo5WIFrAy6SYQe3TibOnpC0jYCchdNS-osgfnp4130_provenance.