Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- befree-2016 importedOn "2016-02-19" NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_assertion wasGeneratedBy ECO_0000203 NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_assertion wasDerivedFrom befree-2016 NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_assertion SIO_000772 21233288 NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_assertion evidence source_evidence_literature NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.
- NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_assertion description "[Our results identify IPIP27A and B as key players in endocytic trafficking and strongly suggest that defects in this process are responsible for the pathology of Lowe syndrome and Dent disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865243.RAOvB_gYRH-ynJrrQe2W4V4o0R53wcbxKvlmDmWGLtsiE130_provenance.