Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_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." NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_assertion evidence source_evidence_literature NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_assertion SIO_000772 9351523 NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_assertion wasDerivedFrom befree-20140225 NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_assertion wasGeneratedBy ECO_0000203 NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718049.RAmTRWkFhQdyJ7FtF6Gw_7TzBLvD4SX37-Bd6-Bh_qHe8130_provenance.