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- source_evidence_literature type ECO_0000212 NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_assertion description "[A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_assertion evidence source_evidence_literature NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_assertion SIO_000772 7757079 NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_assertion wasDerivedFrom befree-2016 NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_assertion wasGeneratedBy ECO_0000203 NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1320846.RAyBAfM-RuEyuwee4Q_sPXrEsZ1ktZy-CVtdidyYB7IwE130_provenance.