Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_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." NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_assertion evidence source_evidence_literature NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_assertion SIO_000772 17216251 NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_assertion wasDerivedFrom befree-2016 NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_assertion wasGeneratedBy ECO_0000203 NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.
- befree-2016 importedOn "2016-02-19" NP588244.RAWpvuz3MH90xMKyBJpcUaqP6m3AK6u4FVtGVWbyt9lss130_provenance.