Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_assertion description "[In the other two families AD PXE could not be confirmed after extensive clinical examinations and application of our criteria, since definite PXE was not present in two or more generations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_assertion evidence source_evidence_curated NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_assertion SIO_000772 15098239 NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_assertion wasDerivedFrom uniprot-2016 NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_assertion wasGeneratedBy ECO_0000218 NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3391.RAvfYEiBUusnr9AkBnuqp7a7XIHEnIPbF3ZhUuG4YFWh8130_provenance.