Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_assertion type Assertion NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_head.
- NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_assertion wasGeneratedBy ECO_0000203 NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_assertion wasDerivedFrom lhgdn-20090331 NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_assertion SIO_000772 17704776 NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_assertion evidence source_evidence_literature NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_assertion description "[Studies show that the clinical features of the reported disorder resemble those of neurofibromatosis type 1 provide the first report of mutations of SPRED1 (SPROUTY)/SPRED family of genes) in human disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.