Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_assertion description "[Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_assertion evidence source_evidence_literature NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_assertion SIO_000772 24903190 NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_assertion wasDerivedFrom befree-20150227 NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_assertion wasGeneratedBy ECO_0000203 NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434547.RA6ZHqrmOlDROsInN_T73NGKAM95lrSHbsfgnD8SBWy_8130_provenance.