Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_assertion description "[Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_assertion evidence source_evidence_literature NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_assertion SIO_000772 9837814 NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_assertion wasDerivedFrom befree-20140225 NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_assertion wasGeneratedBy ECO_0000203 NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925733.RAa84WbB-spwaMn0urkQTx3eI13mzy_ZZCcK3HqXaCaCA130_provenance.