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- source_evidence_literature type ECO_0000212 NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_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." NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_assertion evidence source_evidence_literature NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_assertion SIO_000772 24255920 NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_assertion wasDerivedFrom befree-20150227 NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_assertion wasGeneratedBy ECO_0000203 NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978444.RAz3mqtdb_OjHPJ2gaTw4tPq_7pnjzBEp82-Bz9CTDH00130_provenance.