Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_assertion wasGeneratedBy ECO_0000203 NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_assertion wasDerivedFrom befree-2016 NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_assertion SIO_000772 9758336 NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_assertion evidence source_evidence_literature NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.
- NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_assertion description "[The importance of these developmental findings is bolstered by a recent study which identified mutations in the beta4 as the molecular defect in the mutant epileptic mouse (lethargic; lh/lh).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404950.RAK-E0_nq43vT4M_pd_iLAe4i2o6PADwt83qg55Ib_upE130_provenance.