Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_assertion type Assertion NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_head.
- NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_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." NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.
- NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_assertion evidence source_evidence_curated NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.
- NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_assertion SIO_000772 18006695 NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.
- NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_assertion wasDerivedFrom ctd_human-20150221 NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.
- NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_assertion wasGeneratedBy ECO_0000218 NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.