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- source_evidence_literature type ECO_0000212 NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_assertion description "[Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin-Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_assertion evidence source_evidence_literature NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_assertion SIO_000772 12393804 NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_assertion wasDerivedFrom befree-20140225 NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_assertion wasGeneratedBy ECO_0000203 NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP729165.RAEeVPqE-MX_w2GuNnKwpnjcRqBegmsMguIJOm0azcmp0130_provenance.