Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_assertion description "[Alport syndrome (ATS) is a type-IV collagen inherited disorder, caused by mutations in COL4A3 and COL4A4 (autosomal recessive) or COL4A5 (X-linked).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_assertion evidence source_evidence_literature NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_assertion SIO_000772 23144074 NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_assertion wasDerivedFrom befree-2016 NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_assertion wasGeneratedBy ECO_0000203 NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1027663.RALYcx-zpcg1JFw4USuhwRKZvWI5DYJ8WnwvCWfO7jGS0130_provenance.