Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_assertion> ?p ?o ?g. }
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- NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_assertion type Assertion NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_head.
- NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_assertion description "[Neuroligin mutations most probably represent rare causes of autism; it is unlikely that the allelic variants in any of these genes would be major risk factors for autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_provenance.
- NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_assertion evidence source_evidence_literature NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_provenance.
- NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_assertion SIO_000772 16077734 NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_provenance.
- NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_assertion wasDerivedFrom lhgdn-20090331 NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_provenance.
- NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_assertion wasGeneratedBy ECO_0000203 NP134570.RABHt82OKnEsgHCmA2HXlk_77MZWa7KesaNvsgpiDGzfg130_provenance.