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- source_evidence_literature type ECO_0000212 NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion description "[This study reaffirms the view that large MECP2 deletions are an important cause of both classical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion evidence source_evidence_literature NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion SIO_000772 17712354 NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion wasDerivedFrom lhgdn-20090331 NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion wasGeneratedBy ECO_0000203 NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.