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- NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_assertion type Assertion NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_head.
- NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_assertion wasGeneratedBy ECO_0000203 NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_provenance.
- NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_assertion wasDerivedFrom befree-20150227 NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_provenance.
- NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_assertion SIO_000772 20023659 NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_provenance.
- NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_assertion evidence source_evidence_literature NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_provenance.
- NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_assertion description "[Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939257.RAQi_LV65fzpHsm7a9KrpFSawVgmhrhcmxTDqIGthU5ns130_provenance.