Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_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." NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_assertion evidence source_evidence_literature NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_assertion SIO_000772 18923054 NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_assertion wasDerivedFrom befree-20140225 NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_assertion wasGeneratedBy ECO_0000203 NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.
- befree-20140225 importedOn "2014-02-25" NP315162.RA5-7yDL2Z1x61yAFPhlbAAjaAABVcAg1M85oOXD0B4Os130_provenance.