Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_assertion description "[We report an interstitial deletion of 4q: 46XY der 4 (q28;q35) in a six-year-old boy with dysmorphic features associated with moderate mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_assertion evidence source_evidence_literature NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_assertion SIO_000772 19037546 NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_assertion wasDerivedFrom befree-2016 NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_assertion wasGeneratedBy ECO_0000203 NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.
- befree-2016 importedOn "2016-02-19" NP706117.RAwj4MbPwZTVFpH-16web9gjVOUgHhujroSR4WjOeMFAM130_provenance.