Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_assertion description "[Multiplex XLMR pedigrees have been reported with only one mutated patient having autism and MR: different X-located MR genes have been shown to be involved (NLGN4, MECP2, OPHN1, ZNF674 and FRAXA) which does not suggest that they could be `autism genes`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_assertion evidence source_evidence_literature NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_assertion SIO_000772 19160128 NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_assertion wasDerivedFrom befree-20140225 NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_assertion wasGeneratedBy ECO_0000203 NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP239800.RAxx9oxN__j9e1vW5iAE6nd9htHiclTCG6ubv26gWbaBs130_provenance.