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- source_evidence_literature type ECO_0000212 NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_assertion description "[OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_assertion evidence source_evidence_literature NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_assertion SIO_000772 11440988 NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_assertion wasDerivedFrom befree-2016 NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_assertion wasGeneratedBy ECO_0000203 NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.
- befree-2016 importedOn "2016-02-19" NP323013.RAM0AJxkgsgxA8ujRI_5rrA_04w-yF89_tJr0j7KfQbGo130_provenance.