Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_assertion description "[These new data demonstrate that much of the excess risk of ESRD in African American individuals is attributable to an MYH9 risk haplotype and suggest that hypertension may cause progressive kidney disease only in genetically susceptible individuals or be the result of a primary renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_assertion evidence source_evidence_literature NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_assertion SIO_000772 18923054 NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_assertion wasDerivedFrom befree-2016 NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_assertion wasGeneratedBy ECO_0000203 NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.
- befree-2016 importedOn "2016-02-19" NP698192.RAG2Oh-2UvNQ3MZPqlXwq0huOYk9VPcpOpQMvU7JwFR-w130_provenance.