Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_assertion wasGeneratedBy ECO_0000203 NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_assertion wasDerivedFrom befree-2016 NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_assertion SIO_000772 23206890 NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_assertion evidence source_evidence_literature NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.
- NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_assertion description "[To differentiate severe congenital neutropenia (SCN) from autoimmune neutropenia (AIN) in patients with persistent neutropenia ≤1000/mm(3) over three months, we evaluated anti-neutrophil auto-antibodies, candidate genes of ELANA, HAX1 and GCSFR, and neutrophil elastase (NE) activity in 38 patients (21 females; average onset age 14.12 ± 2.49 months) in a primary immunodeficiency disease center between 2004 and 2011.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1033022.RA-QSW58pU5JrJMtKCVKE3EHDP8aZg_SAhGsxRg6CPjoE130_provenance.