Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_assertion description "[Nine patients belonging to this kindred underwent coagulation study for hereditary thrombophilia, which included plasminogen antigen and activity assays, an activated protein C resistance test, and genetic analysis for factor V Leiden mutation and for prothrombin variant 20210A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_assertion evidence source_evidence_literature NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_assertion SIO_000772 10726047 NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_assertion wasDerivedFrom befree-2016 NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_assertion wasGeneratedBy ECO_0000203 NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.
- befree-2016 importedOn "2016-02-19" NP278523.RAbZreDAdRAciLQKzW406RDyrFl6fvaC_hSM34ZIgkwIA130_provenance.