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- source_evidence_literature type ECO_0000212 NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_assertion description "[We first screened 153 patients with MR and facial dysmorphism associated with malformations, or growth anomalies, or familial history, with cytogenetically normal chromosomes, and the absence of FRAXA mutation and subtelomeric rearrangements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_assertion evidence source_evidence_literature NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_assertion SIO_000772 16773131 NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_assertion wasDerivedFrom befree-2016 NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_assertion wasGeneratedBy ECO_0000203 NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP554498.RAlRmi7KGEM9si-ajiu3U5nEUeh6OVozsE4qYMi9Pk21Q130_provenance.