Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_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." NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_assertion evidence source_evidence_literature NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_assertion SIO_000772 23206890 NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_assertion wasDerivedFrom befree-20140225 NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_assertion wasGeneratedBy ECO_0000203 NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP657541.RAjq0dcul75qKM7NgkFMWuw8Anux1uCKN4PJXCr4j4QMU130_provenance.