Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion description "[We conclude that women homozygous for the Sp1 polymorphism are at significantly increased risk of excess rates of bone loss at the spine, but this effect may be nullified by the use of HRT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion evidence source_evidence_literature NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion SIO_000772 11547832 NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion wasDerivedFrom gad-20130706 NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion wasGeneratedBy ECO_0000203 NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance.