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- source_evidence_literature type ECO_0000212 NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_assertion description "[Furthermore, detailed analysis of PXR1 has revealed that mutations in this gene are responsible for complementation group 2 of the peroxisome biogenesis disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_assertion evidence source_evidence_literature NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_assertion SIO_000772 8993569 NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_assertion wasDerivedFrom befree-20150227 NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_assertion wasGeneratedBy ECO_0000203 NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.
- befree-20150227 importedOn "2015-02-27" NP662473.RAUPMBWYIoC7htyWBRt_5wDphUk6dgELwYb9g933Pvzww130_provenance.