Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_assertion> ?p ?o ?g. }
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- NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_assertion type Assertion NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_head.
- NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_assertion wasGeneratedBy ECO_0000203 NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_provenance.
- NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_assertion wasDerivedFrom befree-20140225 NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_provenance.
- NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_assertion SIO_000772 23532954 NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_provenance.
- NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_assertion evidence source_evidence_literature NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_provenance.
- NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_assertion description "[Pfeiffer syndrome is an autosomal dominant condition classically combining craniosynostosis with digital anomalies of the hands and feet.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368927.RAZA7RgBoA7vLdMRCAWwe2s-ohom_0VRhujwWeLwCSD8g130_provenance.