Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_assertion description "[We screened the FOXG1 gene in a cohort of 206 MECP2 and CDKL5 mutation negative patients (136 females and 70 males) with severe encephalopathy and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_assertion evidence source_evidence_literature NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_assertion SIO_000772 19806373 NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_assertion wasDerivedFrom befree-20150227 NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_assertion wasGeneratedBy ECO_0000203 NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP551933.RA-n1ikLQE91pFdFXa4Ukkb1OS1f0YBLHjR-Pbad0CGGM130_provenance.