Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_assertion description "[In this article, we identify a gene, SLC39A4, located in the candidate region and, in patients with AE, document mutations that likely lead to the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_assertion evidence source_evidence_literature NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_assertion SIO_000772 12032886 NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_assertion wasDerivedFrom befree-2016 NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_assertion wasGeneratedBy ECO_0000203 NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.
- befree-2016 importedOn "2016-02-19" NP356181.RALPL5nt8fu4pWWsVpS7YKKsKM7EH5IKT459R1Q3ZCZNk130_provenance.