Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_assertion wasGeneratedBy ECO_0000203 NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_assertion wasDerivedFrom befree-20150227 NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_assertion SIO_000772 23722637 NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_assertion evidence source_evidence_literature NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.
- NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_assertion description "[Predictive genetic testing of at-risk relatives requires analysis of all CCM genes after identification of an unclassified CCM1 variant in an individual affected with cerebral cavernous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP287539.RAAQ5JHMvWXc7Q46KQx-jx9pvvPQVe9xcGu_iaeCpmgg4130_provenance.