Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_assertion wasGeneratedBy ECO_0000203 NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_assertion wasDerivedFrom befree-20150227 NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_assertion SIO_000772 22054067 NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_assertion evidence source_evidence_literature NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.
- NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_assertion description "[Our findings suggest that genetic variability in members of the GST gene family may be associated with an increased susceptibility to RCC and its progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP987896.RAk--bWBBpf7BHBQ2FWqe7fXTGZObfon82e_H4_PwSMFM130_provenance.