Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_assertion description "[We searched for SLC35D1 mutations in five families with SBD and 15 patients with other SSDD group diseases, including achodrogenesis type 1A, spondylometaphyseal dysplasia Sedaghatian type and fibrochondrogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_assertion evidence source_evidence_literature NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_assertion SIO_000772 19508970 NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_assertion wasDerivedFrom befree-20140225 NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_assertion wasGeneratedBy ECO_0000203 NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876329.RAHAqZKQ8na7jE99BFKq4GSeN_05AbMOF5H3IQJ48LBMk130_provenance.