Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_assertion description "[Laboratory assays are currently available to diagnose and type hereditary thrombophilia due to deficiency or dysfunction of one of the anticoagulant factors antithrombin (AT), protein C (PC) and protein S (PS), and APC resistance without the need of DNA analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_assertion evidence source_evidence_literature NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_assertion SIO_000772 9763348 NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_assertion wasDerivedFrom befree-20140225 NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_assertion wasGeneratedBy ECO_0000203 NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP710118.RA88VKFPvAD6SlSF-l25WZzru_AMKZJiLkjWj9qdPr4Mg130_provenance.