Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_assertion evidence source_evidence_literature NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_assertion SIO_000772 16453125 NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_assertion wasDerivedFrom befree-2016 NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_assertion wasGeneratedBy ECO_0000203 NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.
- befree-2016 importedOn "2016-02-19" NP534197.RAS2QbYaP5QUS0H6eW0RSLKo1l3fzSqfCeyXmpD03ItpY130_provenance.