Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_assertion description "[Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_assertion evidence source_evidence_literature NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_assertion SIO_000772 8765219 NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_assertion wasDerivedFrom befree-20140225 NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_assertion wasGeneratedBy ECO_0000203 NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP352305.RAtJ-P-rOfD8ThOHCvzQqqcoFRB1GuKTxIjdHqnW83Qw4130_provenance.