Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_assertion description "[We assessed 71 children with JMML for NRAS, KRAS, and PTPN11 mutations and evaluated their clinical significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_assertion evidence source_evidence_literature NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_assertion SIO_000772 19047918 NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_assertion wasDerivedFrom befree-20140225 NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_assertion wasGeneratedBy ECO_0000203 NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP530744.RAdAzS9xGVS4Hde1GcnHis319hI39YlL3i6IjgMHGsQX8130_provenance.