Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion> ?p ?o ?g. }
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- NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion type Assertion NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_head.
- NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_provenance.
- NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion evidence source_evidence_literature NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_provenance.
- NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion SIO_000772 17655765 NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_provenance.
- NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion wasDerivedFrom befree-2016 NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_provenance.
- NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion wasGeneratedBy ECO_0000203 NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_provenance.