Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_assertion description "[CYP2C9 and VKORC1 genetic polymorphism analysis might be necessary in patients with Factor V Leiden and prothrombin gene G2021A mutation(s).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_assertion evidence source_evidence_curated NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_assertion SIO_000772 17721328 NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_assertion wasDerivedFrom ctd_human-2016 NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_assertion wasGeneratedBy ECO_0000218 NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP20439.RA_7EUflNJ9XN9Ph1HFj8J4X93DngIP7n9iHL7GiMWsBg130_provenance.