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- source_evidence_literature type ECO_0000212 NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_assertion description "[Further mutation analyses in males with X-linked mental retardation must prove that RSK4 is indeed a novel MRX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_assertion evidence source_evidence_literature NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_assertion SIO_000772 10644430 NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_assertion wasDerivedFrom befree-2016 NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_assertion wasGeneratedBy ECO_0000203 NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.
- befree-2016 importedOn "2016-02-19" NP273063.RAHpn31Ruk-XDemc4LV9Hyi73iB5XuQwX0U2PI91A-9HI130_provenance.