Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_assertion description "[Finally, twelve studies were included for FVL and nine studies were included for G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_assertion evidence source_evidence_literature NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_assertion SIO_000772 24755609 NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_assertion wasDerivedFrom befree-20150227 NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_assertion wasGeneratedBy ECO_0000203 NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP389774.RAktsTN0sD5hogtfJgj3UC9K5cBldLH0C3wLwSYgbtXtE130_provenance.