Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_assertion description "[We performed a mutational analysis of the CHK2 gene using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) in 41 bone marrow samples from individuals with myelodysplastic syndrome (MDS) and 41 samples of acute myeloid leukemias (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_assertion evidence source_evidence_literature NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_assertion SIO_000772 11248330 NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_assertion wasDerivedFrom befree-20140225 NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_assertion wasGeneratedBy ECO_0000203 NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615783.RA3lcpFbZb09fEVXAc-sF3zf1z865pdHUtvNj2Is8UK38130_provenance.