Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_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.
- 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.
- befree-20140225 importedOn "2014-02-25" NP718057.RA6Jq56bW21-Ug7AwvtIt3Do-EH_PliOZ3jJMDRO9O4_8130_provenance.