Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_assertion description "[The current case-control study was aimed to determine the prevalence and the clinical significance of inherited thrombophilia - factor V Leiden and G20210A prothrombin polymorphisms - in patients with antiphospholipid syndrome (APS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_assertion evidence source_evidence_literature NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_assertion SIO_000772 24093662 NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_assertion wasDerivedFrom befree-20150227 NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_assertion wasGeneratedBy ECO_0000203 NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391717.RANY70INcJnnqMJm1QKtvH-w9fesILGD_8alZ6c01wGC0130_provenance.