Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion> ?p ?o ?g. }
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- NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion type Assertion NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_head.
- NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion wasGeneratedBy ECO_0000203 NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_provenance.
- NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion wasDerivedFrom befree-20140225 NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_provenance.
- NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion SIO_000772 18609495 NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_provenance.
- NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion evidence source_evidence_literature NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_provenance.
- NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_assertion description "[Papillorenal syndrome is an autosomal dominant entity due to PAX2 gene mutation, involving optic nerve and renal malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250852.RANtwYne9v2HGr3KxHJ0TRyGjMglxk1mdcSMRX3alR_lw130_provenance.