Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_assertion description "[Our results raise the potential implication of the XPG Asp1104His polymorphism in the occurrence of chromosomal translocations associated with specific subtypes of sarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_assertion evidence source_evidence_literature NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_assertion SIO_000772 16646069 NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_assertion wasDerivedFrom befree-20140225 NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_assertion wasGeneratedBy ECO_0000203 NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP237613.RAnvbuBFkWR0Nb1uHL0Ce46KWx76l_09ZOx_cuZNmExCk130_provenance.