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- source_evidence_literature type ECO_0000212 NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_assertion description "[Two recently published studies demonstrated a strong association of genetic variants in the gene that encodes the molecular motor protein nonmuscle myosin 2a (MYH9) with ESRD in African American patients without diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_assertion evidence source_evidence_literature NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_assertion SIO_000772 18923054 NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_assertion wasDerivedFrom befree-20140225 NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_assertion wasGeneratedBy ECO_0000203 NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP524707.RANcQOywmwaSYkL5dGwAAN0wHRS4lh-5_Z4I8RFEsMSvY130_provenance.