Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_assertion> ?p ?o ?g. }
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- NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_assertion type Assertion NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_head.
- NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_assertion wasGeneratedBy ECO_0000203 NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_provenance.
- NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_assertion wasDerivedFrom befree-20150227 NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_provenance.
- NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_assertion SIO_000772 17139695 NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_provenance.
- NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_assertion evidence source_evidence_literature NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_provenance.
- NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_assertion description "[Eleven paternal diseases were discovered, which were Noonan-like syndrome (1), paternal cervical anomalies (1), Goldenhar syndrome (1), dominant autosomal arthrogryposis (1), osteogenesis imperfecta (3), tuberous sclerosis (1), dominant transposition of great vessels (1), Weyers acrofacial dysostosis (1), and autosomal dominant holoprosencephaly (1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759217.RAJSTqhvLzQXcmZ9VGBmB6_oi2TOZlRAXY4Xhv_RCOVQg130_provenance.