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- source_evidence_literature type ECO_0000212 NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_assertion wasGeneratedBy ECO_0000203 NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_assertion wasDerivedFrom befree-20150227 NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_assertion SIO_000772 21926154 NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_assertion evidence source_evidence_literature NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.
- NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_assertion description "[Presently, guidelines for FMR1 genetic testing includes early menopause, congenital intellectual disability, autism spectrum disorder, tremor or ataxia, and a family history of FXTAS or fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408769.RAzkBDi426XQiOUudTJaSgqeErfjHw9vh8Fifw0PPCMSs130_provenance.