Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_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." NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_assertion evidence source_evidence_literature NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_assertion SIO_000772 23206890 NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_assertion wasDerivedFrom befree-20150227 NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_assertion wasGeneratedBy ECO_0000203 NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP843753.RA93hyRPp_HRJ_dI-I452rTG6oNSpF4XkC5TzqdmM8tA4130_provenance.