Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_assertion> ?p ?o ?g. }
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- NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_assertion type Assertion NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_head.
- 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.
- NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_assertion evidence source_evidence_literature NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.
- NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_assertion SIO_000772 16613994 NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.
- NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_assertion wasDerivedFrom befree-20140225 NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.
- NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_assertion wasGeneratedBy ECO_0000203 NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.