Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_assertion description "[Using genome-wide association methodology, we have successfully identified a SNP in complete LD with a sequence variant previously shown to be strongly associated with factor VII, providing proof of principle for this approach. Further study of additional]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_assertion evidence source_evidence_literature NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_assertion SIO_000772 17903294 NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_assertion wasDerivedFrom gad-20150221 NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_assertion wasGeneratedBy ECO_0000203 NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP156611.RAIi7uO2yoec15ts6YjxULzIiqdLz2-P99hfu6MPNDXJ0130_provenance.