Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_assertion> ?p ?o ?g. }
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- NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_assertion type Assertion NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_head.
- NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_assertion wasGeneratedBy ECO_0000203 NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_provenance.
- NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_assertion wasDerivedFrom befree-2016 NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_provenance.
- NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_assertion SIO_000772 17139695 NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_provenance.
- NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_assertion evidence source_evidence_literature NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_provenance.
- NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_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." NP581960.RA7kENzIRYz9fOuKi8wC5kQGN7ftyQvq4IpNNlVJmj0i0130_provenance.