Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_assertion description "[The presence of the CCR5Delta32 allele in recipients constituted an independent and protective factor associated with a decreased risk of GvHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_assertion evidence source_evidence_literature NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_assertion SIO_000772 17145599 NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_assertion wasDerivedFrom befree-20150227 NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_assertion wasGeneratedBy ECO_0000203 NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP316881.RAHExQ2Q9rVLleErpctRg-gxzGtz-HvaxcpkgiCfqeaTE130_provenance.