Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_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." NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_assertion evidence source_evidence_literature NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_assertion SIO_000772 2647943 NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_assertion wasDerivedFrom befree-20140225 NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_assertion wasGeneratedBy ECO_0000203 NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485293.RA5OpqTWD3iTZNbO2SN89-b6EU2pvKV3xdXdaqB-cjriE130_provenance.