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- source_evidence_literature type ECO_0000212 NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP228331.RAotK2dq1ricxUCI_-aRkknVkdf_NG-otuBWE8oKqkmDY130_provenance.
- 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.