Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_assertion description "[In our present study, we examined EphA2 and p53 status (both expression and full-length mutation status) in 6 ovarian cell lines and 79 human ovarian cancers to determine potential associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_assertion evidence source_evidence_literature NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_assertion SIO_000772 16969087 NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_assertion wasDerivedFrom befree-2016 NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_assertion wasGeneratedBy ECO_0000203 NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.
- befree-2016 importedOn "2016-02-19" NP569017.RAgK7JwqU_QfpOlYTLOQEHkWILX8RtFgs75rVmoonrWyk130_provenance.