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- source_evidence_literature type ECO_0000212 NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- befree-2016 importedOn "2016-02-19" NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_assertion wasGeneratedBy ECO_0000203 NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_assertion wasDerivedFrom befree-2016 NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_assertion SIO_000772 12719401 NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_assertion evidence source_evidence_literature NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.
- NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_assertion description "[Sporadic case of fatal encephalopathy with neonatal onset associated with a T158M missense mutation in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392607.RAutDHmUxdDN6LjeDXfChEWKEOUcPiNfv5XfyOxWDi1-8130_provenance.