Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_assertion description "[In conclusion, the NOS3 and Cav1 polymorphisms were significantly associated with the risk of SSNHL and M�ni�re's disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_assertion evidence source_evidence_literature NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_assertion SIO_000772 23560644 NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_assertion wasDerivedFrom befree-2016 NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_assertion wasGeneratedBy ECO_0000203 NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1066853.RAfmOAGnj_Z5sM6fT7rER5ulxKrd_vADZcVvDMhh3N6zE130_provenance.