Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_assertion description "[Deficiencies of coagulation factors other than factor VIII and factor IX (afibrinogenemia, FII, FV, FV+FVIII, FVII, FX, FXI, FXIII) that cause bleeding disorders (RBDs) are inherited as autosomal recessive traits and are rare, with prevalences in the general population varying between 1 in 500,000 and 1 in 2 million for the homozygous forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_assertion evidence source_evidence_literature NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_assertion SIO_000772 16684009 NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_assertion wasDerivedFrom befree-2016 NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_assertion wasGeneratedBy ECO_0000203 NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.
- befree-2016 importedOn "2016-02-19" NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.