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- source_evidence_curated type ECO_0000205 NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.
- 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.
- ctd_human-20150221 importedOn "2015-02-21" NP26367.RAiaRHyXbwTAtAXGm_GZE4C4NE2hKEovX9ZHkLFAN1XBw130_provenance.