Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- befree-2016 importedOn "2016-02-19" NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_assertion wasGeneratedBy ECO_0000203 NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_assertion wasDerivedFrom befree-2016 NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_assertion SIO_000772 21907713 NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_assertion evidence source_evidence_literature NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.
- NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_assertion description "[Mutations in HCCS on the C-terminal side of the CP motifs, known to cause disease states in humans (microphthalmia with linear skin defects) abolished or drastically attenuated holocytochrome c production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922762.RAGKhhdm2IP1Pm-Smmx-1B1W5ltNq6ZTbQtHiXk7vCsh0130_provenance.