Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- 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." provenance.
- 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." provenance.
- NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_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." NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.
- NP391463.RAZIi-xt91pudJR0T5s1MOvQsBj8-3MYzdjMIeqaG7-uM130_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." NP391463.RAZIi-xt91pudJR0T5s1MOvQsBj8-3MYzdjMIeqaG7-uM130_provenance.
- NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_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." NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_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.
- NP544845.RAIz88V92THX2vO0xczceevApOhziEfPNnKx2IBCJnHug130_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." NP544845.RAIz88V92THX2vO0xczceevApOhziEfPNnKx2IBCJnHug130_provenance.