Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_assertion description "[Because common genetic variants can alter the expression or function of MMPs, we hypothesized that potentially functional single-nucleotide polymorphisms (SNPs) in the MMP9 gene may be associated with the survival of patients with invasive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_assertion evidence source_evidence_literature NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_assertion SIO_000772 23570558 NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_assertion wasDerivedFrom befree-20150227 NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_assertion wasGeneratedBy ECO_0000203 NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP564919.RA-e_1bVF8YqnwNLTWZna0cYow8R5qdLn8s1h4QvPUcSM130_provenance.