Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1154064.RAj7Hc8ZpqQcb-k6PAYhrH8gOIQKMWIAd8inW1h635YnE#assertion> ?p ?o ?g. }
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- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion SIO_000772 23144470 provenance.
- assertion evidence source_evidence_literature provenance.
- assertion description "[The molecular cause of autosomal dominant familial PHP1b has been well-defined with identification of microdeletions within the GNAS locus or the nearby STX16, but the molecular mechanism of the GNAS imprinting defects in sporadic PHP1b cases remains elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.