Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_assertion description "[Two independent association samples of 271 AD patients and 280 representative controls were investigated whether the risk for developing AD is altered in carriers of polymorphisms in the alpha2M-gene (Va1000Ile), in the LRP-gene (Ala216Val) and in the RAP-gene (Val311Met).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_assertion evidence source_evidence_literature NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_assertion SIO_000772 16650578 NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_assertion wasDerivedFrom gad-20150221 NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_assertion wasGeneratedBy ECO_0000203 NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69461.RA7nuTnPfbDKLtWcMy3j4pM6g-L11yCaJrkoGg0kMiJNQ130_provenance.