Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_assertion wasGeneratedBy ECO_0000203 NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_assertion wasDerivedFrom befree-20150227 NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_assertion SIO_000772 16015425 NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_assertion evidence source_evidence_literature NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.