Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_assertion description "[For confirmation of homozygous protein C deficiency in a neonate with purpura fulminans or massive venous thrombosis, the infant should have undetectable protein C activity and both parents should be heterozygous for protein C deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_assertion evidence source_evidence_literature NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_assertion SIO_000772 2647943 NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_assertion wasDerivedFrom befree-20140225 NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_assertion wasGeneratedBy ECO_0000203 NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP219332.RALesKxDopSYTnGUEC1xquQ8tfOgbKB7xvH_Axx8OtBSk130_provenance.