Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_assertion description "[It was previously found to be highly sensitive for the factor V Leiden mutation and for protein C deficiency, but only moderately sensitivity for protein S deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_assertion evidence source_evidence_literature NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_assertion SIO_000772 11685046 NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_assertion wasDerivedFrom gad-20150221 NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_assertion wasGeneratedBy ECO_0000203 NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP71801.RAUl1VquerRdW7yhFWn8gPY7R90oBXFrN8IOxtlwEs8C4130_provenance.