Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion description "[The apoE4 targeted replacement mice do not harbor any mutation in the amyloid precursor protein gene and, therefore, are similar to the majority of humans susceptible to cerebral amyloid angiopathy and ICH, where the APOE genetic polymorphism is the only known genetic risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion evidence source_evidence_literature NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion SIO_000772 18755411 NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion wasDerivedFrom befree-20140225 NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion wasGeneratedBy ECO_0000203 NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance.