Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_assertion description "[We compared the 48 NP-FDC patients with a sample of 96 patients with sporadic DCM, who were randomly matched by year of enrolment in a 2:1 ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_assertion evidence source_evidence_literature NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_assertion SIO_000772 20525703 NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_assertion wasDerivedFrom befree-20140225 NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_assertion wasGeneratedBy ECO_0000203 NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP860141.RAO22ocTLSZeY4xvBZSMUHWaZGd_aPnwBrGZlHynawwhY130_provenance.