Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP544844.RAtoBc05qeeOvJ-AiT_iNhNnDXNQJgOWJ6WJ6rh1vsKow130_provenance.