Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_assertion wasGeneratedBy ECO_0000203 NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_assertion wasDerivedFrom befree-20140225 NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_assertion SIO_000772 16237566 NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_assertion evidence source_evidence_literature NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_assertion description "[Autosomal-recessive Schimke immuno-osseous dysplasia (SIOD) characterized by spondyloepiphyseal dysplasia, focal-segmental glomerulosclerosis (FSGS), T-cell immunodeficiency and facial dysmorphism is caused by defects in the SMARCAL1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP894813.RA4GJgQsCcmh2Qx5ucdatlsgoSUTN8F3gBWxvAtwOXGPw130_provenance.