Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_assertion> ?p ?o ?g. }
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- NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_assertion type Assertion NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_head.
- NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_assertion description "[The two males and the two obligate carrier females presented a mutation in the MECP2 gene, demonstrating that, in males, MECP2 can be responsible for severe mental retardation associated with neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_provenance.
- NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_assertion evidence source_evidence_literature NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_provenance.
- NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_assertion SIO_000772 10986043 NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_provenance.
- NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_assertion wasDerivedFrom befree-2016 NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_provenance.
- NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_assertion wasGeneratedBy ECO_0000203 NP294995.RAiVt0Dt5dFgQaZXl0bEq2_KONakUije6QUbZYcf9ctlw130_provenance.