Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_assertion type Assertion NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_head.
- NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_assertion wasGeneratedBy ECO_0000218 NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_provenance.
- NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_assertion wasDerivedFrom ctd_human-20130708 NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_provenance.
- NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_assertion SIO_000772 20023659 NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_provenance.
- NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_assertion evidence source_evidence_curated NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_provenance.
- NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_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." NP20202.RAYucr0vnckZrt0W_3W5F5Z0U597SuOi7I7zPlskOk6_c130_provenance.