Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_assertion wasGeneratedBy ECO_0000203 NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_assertion wasDerivedFrom befree-20140225 NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_assertion SIO_000772 22872102 NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_assertion evidence source_evidence_literature NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_assertion description "[Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297707.RA5g_mfS5zfbGciPmcrI729PDTKC8ycoMYhG5NS-pmXEg130_provenance.