Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_assertion wasGeneratedBy ECO_0000203 NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_assertion wasDerivedFrom befree-20150227 NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_assertion SIO_000772 8972002 NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_assertion evidence source_evidence_literature NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.
- NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_assertion description "[Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641675.RAjLbrJ2z--KIdJqZsx-UKL96Ayp9fBj42lIGvZIITWbI130_provenance.