Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- befree-2016 importedOn "2016-02-19" NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_assertion wasGeneratedBy ECO_0000203 NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_assertion wasDerivedFrom befree-2016 NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_assertion SIO_000772 11576738 NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_assertion evidence source_evidence_literature NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.
- NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_assertion description "[PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331334.RA303vugiulz0_VC9RmX_rwkDONh5wZsOnNlkQk9Tmkqo130_provenance.