Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_assertion> ?p ?o ?g. }
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- NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_assertion type Assertion NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_head.
- 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.
- NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_assertion evidence source_evidence_literature NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_provenance.
- NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_assertion SIO_000772 16613994 NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_provenance.
- NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_assertion wasDerivedFrom befree-2016 NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_provenance.
- NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_assertion wasGeneratedBy ECO_0000203 NP544842.RABgXfE0UsBsL8JUaQWqcM7fIMoNiWOuVofhmwguxfV3s130_provenance.