Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_assertion type Assertion NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_head.
- NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_assertion description "[The factor V Leiden (FVL) mutation is the most common cause of inherited thrombophilia in Caucasian populations, and women with this variant allele are at increased risk for pregnancy complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.
- NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_assertion evidence source_evidence_literature NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.
- NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_assertion SIO_000772 16613994 NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.
- NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_assertion wasDerivedFrom befree-2016 NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.
- NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_assertion wasGeneratedBy ECO_0000203 NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.