Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_assertion description "[Also for an 18-bp deletion in the promoter of VEGF a significant difference in the genotype and allele frequencies was observed between the KD patients and the controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_assertion evidence source_evidence_literature NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_assertion SIO_000772 16645995 NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_assertion wasDerivedFrom befree-20140225 NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_assertion wasGeneratedBy ECO_0000203 NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506350.RAdi9RaShNi9O4vJNc169aMANQqvPEmMSFBSvOZDh9YlE130_provenance.