Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_assertion> ?p ?o ?g. }
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- NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_assertion type Assertion NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_head.
- NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_assertion wasGeneratedBy ECO_0000203 NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_provenance.
- NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_assertion wasDerivedFrom befree-2016 NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_provenance.
- NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_assertion SIO_000772 19349604 NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_provenance.
- NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_assertion evidence source_evidence_literature NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_provenance.
- NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_assertion description "[In those with p.R168X, a commonly occurring MECP2 mutation in RTT, there was a 6-point increase in severity score for those who were heterozygous for the BDNF polymorphism, both unadjusted (p = 0.02) and adjusted for age (p = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730832.RAGxNF0pKiPxYzW5FbwO6H1yNAscKu2G1ElfdYR6-gF-U130_provenance.