Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_assertion description "[Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_assertion evidence source_evidence_literature NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_assertion SIO_000772 17721994 NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_assertion wasDerivedFrom gad-20150221 NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_assertion wasGeneratedBy ECO_0000203 NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP111088.RAxFglWLpGLjXmKf8EoFaIjM-vG6ym4yrkXNLm4Fa9_XE130_provenance.