Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_assertion description "[The factor V mutation was more common in CRVO (3/40, 8%) than controls (0/79, 0%), P = .036, as was high (>150%) factor VIII (12/40, 30%) versus (4/77, 5%), P = .0002.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_assertion evidence source_evidence_literature NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_assertion SIO_000772 18160589 NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_assertion wasDerivedFrom befree-20150227 NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_assertion wasGeneratedBy ECO_0000203 NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.
- befree-20150227 importedOn "2015-02-27" NP323070.RAn69gYftPUGZy_TFAUjuD8ItmNU6wu_pghDKiVkvlBis130_provenance.