Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_assertion description "[We suggest naming this variant of coproporphyrinogen oxidase defect `harderoporphyria.`]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_assertion evidence source_evidence_literature NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_assertion SIO_000772 6886003 NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_assertion wasDerivedFrom befree-20140225 NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_assertion wasGeneratedBy ECO_0000203 NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP694270.RATOMu1Ir5MDqAvlu_UfF41s8xreY0cEWMN4SRKeUPwsQ130_provenance.