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- source_evidence_literature type ECO_0000212 NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_assertion description "[The aberrant fibrillin-1 staining observed in this study is similar to that observed in Marfan syndrome, a syndrome caused by mutations in the gene encoding fibrillin-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_assertion evidence source_evidence_literature NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_assertion SIO_000772 18084245 NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_assertion wasDerivedFrom befree-2016 NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_assertion wasGeneratedBy ECO_0000203 NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.
- befree-2016 importedOn "2016-02-19" NP645511.RAISQPoNdM1kIKLClV_ENFTdMqvNaAVToV9VjwhmvGIuk130_provenance.