Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_assertion description "[Dystrophin assays should be employed whenever the diagnosis of fetal DMD is equivocal (e.g., cases in which a gene deletion cannot be identified).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_assertion evidence source_evidence_literature NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_assertion SIO_000772 2672800 NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_assertion wasDerivedFrom befree-2016 NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_assertion wasGeneratedBy ECO_0000203 NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295860.RAyVqgevreQ4L1tqTDzAIXLj5zumaDCaiqiLkfmcNQSqk130_provenance.