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- source_evidence_literature type ECO_0000212 NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_assertion description "[We show that Asxl1 deletion in mice led to developmental abnormalities including dwarfism, anophthalmia, and 80% embryonic lethality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_assertion evidence source_evidence_literature NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_assertion SIO_000772 24255920 NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_assertion wasDerivedFrom befree-2016 NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_assertion wasGeneratedBy ECO_0000203 NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1129844.RAoXlw7hox1HRSi-wiqiwx8M8-p1upRXwUe5JGBeVvfr8130_provenance.