Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_assertion description "[PATIENTS, DESIGN AND MEASUREMENTS: The CaR gene from FHH family members was assessed for mutations by direct DNA sequencing and mutations were confirmed by restriction enzyme analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_assertion evidence source_evidence_literature NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_assertion SIO_000772 16649980 NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_assertion wasDerivedFrom befree-20140225 NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_assertion wasGeneratedBy ECO_0000203 NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189704.RAQeVO3LD0MAXZIQiVoCkVytDobx1MLKTKbFlZutl8ivU130_provenance.