Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_assertion wasGeneratedBy ECO_0000203 NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_assertion wasDerivedFrom befree-2016 NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_assertion SIO_000772 23798676 NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_assertion evidence source_evidence_literature NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.
- NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_assertion description "[These data provide new insights into the formation and activities of CCN1-truncated variants and raise the predictive value of the form containing completely or partially the IGFBP and vWC domains as a surrogate marker of CCN1 activity in PDR distinguishing pathological from physiological angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1088761.RArxL8RiTfEuADHHXIQHQS3_MxpS2h6NBdnpZ-qyr9g_k130_provenance.