Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_assertion> ?p ?o ?g. }
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- NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_assertion type Assertion NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_head.
- NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_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." NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.
- NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_assertion evidence source_evidence_literature NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.
- NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_assertion SIO_000772 10986043 NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.
- NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_assertion wasDerivedFrom befree-20140225 NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.
- NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_assertion wasGeneratedBy ECO_0000203 NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.