Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_assertion evidence source_evidence_literature NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_assertion SIO_000772 11439091 NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_assertion wasDerivedFrom befree-2016 NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_assertion wasGeneratedBy ECO_0000203 NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- befree-2016 importedOn "2016-02-19" NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.