Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_assertion description "[The high frequency of ARDS in patients with MTP defects suggests that this inborn error may be a risk factor for ARDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_assertion evidence source_evidence_literature NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_assertion SIO_000772 14605499 NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_assertion wasDerivedFrom befree-20140225 NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_assertion wasGeneratedBy ECO_0000203 NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP779165.RAMLah52Rct5FMw5wLDFZqDW6gFlTuGwVxoahMKamWfPQ130_provenance.