Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_assertion description "[In addition, six novel polymorphisms (G455G, I462I, G736G and IVS 38-8 G>A in COL4A3, and L658L and A1577A in COL4A4) were demonstrated.Many different COL4A3 and COL4A4 mutations cause TBMN and autosomal recessive Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_assertion evidence source_evidence_literature NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_assertion SIO_000772 17216251 NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_assertion wasDerivedFrom befree-20140225 NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_assertion wasGeneratedBy ECO_0000203 NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP161213.RAt8MXuGLkOrtjcXkER7XOcZveY8msqhp7-XAb_enNeEo130_provenance.