Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_assertion wasGeneratedBy ECO_0000203 NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_assertion wasDerivedFrom befree-20150227 NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_assertion SIO_000772 22015311 NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_assertion evidence source_evidence_literature NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.
- NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_assertion description "[Mutation analysis of the optineurin gene in familial amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837085.RADOf8H6T8-m8nBHPZvC2qsE4r_BCjbYCwn2x_2C5T6UA130_provenance.