Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion> ?p ?o ?g. }
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- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion type Assertion NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_head.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion evidence source_evidence_literature NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion SIO_000772 10852374 NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion wasDerivedFrom befree-20150227 NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion wasGeneratedBy ECO_0000203 NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.