Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- befree-2016 importedOn "2016-02-19" NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_assertion wasGeneratedBy ECO_0000203 NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_assertion wasDerivedFrom befree-2016 NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_assertion SIO_000772 22015311 NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_assertion evidence source_evidence_literature NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.
- NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_assertion description "[Mutations in the optineurin gene (OPTN) have been reported in rare familial and sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932494.RARqrhs7g5GbjH4MiANb5jN9HfJHH9wXDWoohtLv7uMIE130_provenance.