Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_assertion description "[As there is increasing evidence that CENPF is associated with poor prognosis in patients with primary BC, further independent studies are needed to clarify the importance of genetic variation in the CENPF gene in the clinic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_assertion evidence source_evidence_literature NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_assertion SIO_000772 19008095 NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_assertion wasDerivedFrom befree-20150227 NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_assertion wasGeneratedBy ECO_0000203 NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.
- befree-20150227 importedOn "2015-02-27" NP310438.RAHRKUu_H5-B0UYP_40YDRz9zLolz7ESt9pHI5PAZGrig130_provenance.