Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion> ?p ?o ?g. }
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- NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion type Assertion NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_head.
- NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_provenance.
- NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion evidence source_evidence_literature NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_provenance.
- NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion SIO_000772 21858451 NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_provenance.
- NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion wasDerivedFrom befree-20140225 NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_provenance.
- NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion wasGeneratedBy ECO_0000203 NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_provenance.