Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_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." NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_assertion evidence source_evidence_curated NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_assertion SIO_000772 18006695 NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_assertion wasDerivedFrom ctd_human-20130708 NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_assertion wasGeneratedBy ECO_0000218 NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP26489.RAqpLdP3-WkLpLyXAhQ8U12sf39EM7Em10ulPmNiWWlYg130_provenance.