Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_assertion description "[Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_assertion evidence source_evidence_literature NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_assertion SIO_000772 23686771 NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_assertion wasDerivedFrom befree-2016 NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_assertion wasGeneratedBy ECO_0000203 NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1078848.RAY8Jf5hgG-OpRMwgyr2FKZGaqfoGCYL_IHBF-jpsLwR4130_provenance.