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- source_evidence_literature type ECO_0000212 NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_assertion evidence source_evidence_literature NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_assertion SIO_000772 19524642 NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_assertion wasDerivedFrom befree-20150227 NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_assertion wasGeneratedBy ECO_0000203 NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.