Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_assertion evidence source_evidence_literature NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_assertion SIO_000772 11439091 NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_assertion wasDerivedFrom befree-2016 NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_assertion wasGeneratedBy ECO_0000203 NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- befree-2016 importedOn "2016-02-19" NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.