Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_assertion description "[Copy number variation of FCGR3A rather than FCGR3B and FCGR2B is associated with susceptibility to anti-GBM disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_assertion evidence source_evidence_literature NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_assertion SIO_000772 19946017 NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_assertion wasDerivedFrom befree-2016 NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_assertion wasGeneratedBy ECO_0000203 NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.
- befree-2016 importedOn "2016-02-19" NP778277.RAUWrfnV_Vg4H7qoHSHp3a5qXn1FpXGxA2R8-OB_weBlI130_provenance.