Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_assertion description "[Homozygous individuals usually develop purpura fulminans as newborns; heterozygous protein C-deficient individuals are at increased risk for venous thrombosis and pulmonary embolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_assertion evidence source_evidence_literature NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_assertion SIO_000772 2195715 NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_assertion wasDerivedFrom befree-20140225 NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_assertion wasGeneratedBy ECO_0000203 NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP936602.RAZxfVLACC5R7M6ukM7wtlAdFV-xT5B407mWfeAklQU_U130_provenance.