Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP296321.RAg981pUG4PTufOqHyLx7LAEMgzlRL-h0DeqI2tpyvfX0130_provenance.