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- source_evidence_literature type ECO_0000212 NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_assertion description "[The association of the rare C4B3 variant with microangiopathy suggests a genetic component of its aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_assertion evidence source_evidence_literature NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_assertion SIO_000772 3926068 NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_assertion wasDerivedFrom befree-2016 NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_assertion wasGeneratedBy ECO_0000203 NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1304164.RAwHkZ-KBQ-h8l5iMaqlzaRsR3BVc3TSDoB4x_1Amgw9I130_provenance.