Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_assertion description "[Furthermore, we suggest that the diagnosis should be refined to, for example, NS-PTPN11-associated or CFC-BRAF-associated syndromes after the genetic defect has been established, as this may affect the prognosis and treatment of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_assertion evidence source_evidence_literature NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_assertion SIO_000772 18456719 NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_assertion wasDerivedFrom befree-20150227 NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_assertion wasGeneratedBy ECO_0000203 NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP660710.RA_nPtPsuhoS2pExj6ZMo_Fs4--2bQPWFTih33sWDYbZU130_provenance.