Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_assertion> ?p ?o ?g. }
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- NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_assertion type Assertion NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_head.
- NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_assertion description "[A genetic defect is evident in some cases; known genetic changes include: multiple endocrine neoplasia type 1 (MEN1); Carney complex; McCune-Albright syndrome; and, more recently identified, aryl hydrocarbon receptor-interacting protein (AIP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_provenance.
- NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_assertion evidence source_evidence_literature NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_provenance.
- NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_assertion SIO_000772 22024364 NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_provenance.
- NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_assertion wasDerivedFrom befree-20140225 NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_provenance.
- NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_assertion wasGeneratedBy ECO_0000203 NP443878.RAG2LqxGIIncuK-45zKFeKC3Qck6xL3B8p6qlLarApvUk130_provenance.