Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_assertion evidence source_evidence_literature NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_assertion SIO_000772 22095278 NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_assertion wasDerivedFrom befree-20140225 NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_assertion wasGeneratedBy ECO_0000203 NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP710263.RAKZ-0JhM9QvQQNj4WxZ4CAKC8d2MmRyl-tvak4Dqf4Nw130_provenance.