Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- befree-2016 importedOn "2016-02-19" NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_assertion wasGeneratedBy ECO_0000203 NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_assertion wasDerivedFrom befree-2016 NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_assertion SIO_000772 11891694 NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_assertion evidence source_evidence_literature NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.
- NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_assertion description "[A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.