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- source_evidence_literature type ECO_0000212 NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_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." NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_assertion evidence source_evidence_literature NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_assertion SIO_000772 11439091 NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_assertion wasDerivedFrom befree-20150227 NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_assertion wasGeneratedBy ECO_0000203 NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.