Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_assertion description "[Recently, LSP1 was identified as the 47-kD protein overexpressed in the polymorphonuclear neutrophils of patients with a rare neutrophil disorder, neutrophil actin dysfunction with abnormalities of 47-kD and 89-kD proteins (NAD 47/89).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_assertion evidence source_evidence_literature NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_assertion SIO_000772 9616178 NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_assertion wasDerivedFrom befree-20150227 NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_assertion wasGeneratedBy ECO_0000203 NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP250622.RArsnHa7PScjuYaWRNuHGNwhSg1gXk5PH7Jes-sD0SiBU130_provenance.