Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_assertion> ?p ?o ?g. }
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- NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_assertion type Assertion NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_head.
- NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_assertion wasGeneratedBy ECO_0000203 NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_provenance.
- NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_assertion wasDerivedFrom befree-20150227 NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_provenance.
- NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_assertion SIO_000772 17704776 NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_provenance.
- NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_assertion evidence source_evidence_literature NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_provenance.
- NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_assertion description "[Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977298.RAX9PV_wOMvwVT_VWIoRuOf7yJRboMqpeuQbYf2roJ2rk130_provenance.