Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_assertion> ?p ?o ?g. }
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- NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_assertion type Assertion NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_head.
- NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_assertion description "[Scan of 977 nonsynonymous SNPs in CLL4 trial patients for the identification of genetic variants influencing prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_provenance.
- NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_assertion evidence source_evidence_literature NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_provenance.
- NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_assertion SIO_000772 18006695 NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_provenance.
- NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_assertion wasDerivedFrom gad-20150221 NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_provenance.
- NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_assertion wasGeneratedBy ECO_0000203 NP115238.RAlfB83nDE7mKX4PGWP-UeWdcVdm1uBRrriOmm61Mv6pw130_provenance.