Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_assertion description "[SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_assertion evidence source_evidence_literature NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_assertion SIO_000772 22292843 NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_assertion wasDerivedFrom befree-2016 NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_assertion wasGeneratedBy ECO_0000203 NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.
- befree-2016 importedOn "2016-02-19" NP957389.RAgeM-6BQmuNJwd6aVhxgesr2GrVgO2KA-CdM-FS0LL-I130_provenance.