Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_assertion description "[All four patients have epilepsy and a more severe degree of mental retardation than is usual in fragile X syndrome resulting from FMR1 triplet repeat expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_assertion evidence source_evidence_literature NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_assertion SIO_000772 10424820 NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_assertion wasDerivedFrom befree-2016 NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_assertion wasGeneratedBy ECO_0000203 NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP258810.RAA9KiwDmxOh_9esYbVR_5Rwri738UWMWbds1SUlSIE-k130_provenance.