Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_assertion description "[Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_assertion evidence source_evidence_literature NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_assertion SIO_000772 16261289 NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_assertion wasDerivedFrom gad-20150221 NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_assertion wasGeneratedBy ECO_0000203 NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.
- gad-20150221 importedOn "2015-02-21" NP96801.RADANV4WoB1Dm19nbG8LRXFbqJpqAuDmb2djxvMSH5u-Y130_provenance.