Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_assertion description "[These data suggest that the imperfect CT repeat in PIP5K2A intron 9 should be further investigated as a possible candidate allele for 10p12-linked psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_assertion evidence source_evidence_literature NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_assertion SIO_000772 14582145 NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_assertion wasDerivedFrom gad-20150221 NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_assertion wasGeneratedBy ECO_0000203 NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP66529.RAZ6c3yviSYVo0jPqFuSu3b7WtdYX5iFETEzxcC2RxVhs130_provenance.