Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_assertion description "[The underlying etiologies are less well-defined; however, the disorders of factor XII deficiency, dysfibrinogenemia, Wien-Penzing platelet defect, and sticky platelet syndrome (SPS) are treatable inherited thrombophilias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_assertion evidence source_evidence_literature NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_assertion SIO_000772 10548072 NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_assertion wasDerivedFrom befree-20140225 NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_assertion wasGeneratedBy ECO_0000203 NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP842614.RAik2AQvW9gfcRqQ_HOqHsX-nRDCBFDdAJjA1lvn81YvI130_provenance.