Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_assertion> ?p ?o ?g. }
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- NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_assertion type Assertion NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_head.
- NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_assertion description "[In addition, we analyzed five patients with BFPP who did not show GPR56 mutation and found that they define a clinically, radiographically, and genetically distinct syndrome that we termed BFPP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_provenance.
- NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_assertion evidence source_evidence_literature NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_provenance.
- NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_assertion SIO_000772 16240336 NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_provenance.
- NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_assertion wasDerivedFrom befree-2016 NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_provenance.
- NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_assertion wasGeneratedBy ECO_0000203 NP518970.RAnS8hN8XMHPQVbVbVGHNOWFatgssVBWVtuMjvMSRqyKQ130_provenance.