Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_assertion evidence source_evidence_literature NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_assertion SIO_000772 11309367 NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_assertion wasDerivedFrom befree-20140225 NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_assertion wasGeneratedBy ECO_0000203 NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.