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- source_evidence_literature type ECO_0000212 NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_assertion description "[In addition to the support for previously identified loci (PTPN22/1p13; ERBB3/12q13; SH2B3/12q24; CLEC16A/16p13; UBASH3A/21q22), evidence supporting two new and distinct chromosome locations associated with T1D was observed: FHOD3/18q12 (rs2644261, P=5.9 x 10(-4)) and Xp22 (rs5979785, P=6.8 x 10(-3); http://www.T1DBase.org).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_assertion evidence source_evidence_literature NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_assertion SIO_000772 19956107 NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_assertion wasDerivedFrom befree-20140225 NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_assertion wasGeneratedBy ECO_0000203 NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP289542.RA7XjHmW94BxNxFrDk9UCJ6ZaUoUXIzfQ-yVFrRoi4oeE130_provenance.