Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_assertion description "[Automated fluorescence-based DNA sequence analysis of amplified genomic DNA was used to define prothrombin gene regions from a patient with severe functional hypoprothrombinemia and little detectable prothrombin antigen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_assertion evidence source_evidence_literature NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_assertion SIO_000772 9351523 NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_assertion wasDerivedFrom befree-2016 NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_assertion wasGeneratedBy ECO_0000203 NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1382962.RAdE05vu7UQbOXkuMpf22dH9r2X9ZFY8JcoEsLJEl57oI130_provenance.