Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_assertion> ?p ?o ?g. }
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- NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_assertion type Assertion NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_head.
- NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_assertion wasGeneratedBy ECO_0000203 NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_provenance.
- NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_assertion wasDerivedFrom befree-20150227 NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_provenance.
- NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_assertion SIO_000772 15319456 NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_provenance.
- NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_assertion evidence source_evidence_literature NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_provenance.
- NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_assertion description "[Mutations of CD40, the receptor for CD40L, cause a rare autosomal form of HIGM with a clinical phenotype similar to CD40L deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294786.RAS0aCy7v1t4H6YzkF3DUDqqbXWR1W0ZZ3zu4dQMubtyc130_provenance.