Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_assertion description "[The distribution of the GpIIIa A1/A2 polymorphism in patients with SVD stroke and CE stroke was similar to that of their controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_assertion evidence source_evidence_literature NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_assertion SIO_000772 15178823 NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_assertion wasDerivedFrom befree-20150227 NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_assertion wasGeneratedBy ECO_0000203 NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP522833.RA_0NmBkbBXw_funX0CRjSzjZWZ-tZprOnG3R4ZcexlD0130_provenance.