Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_assertion description "[Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_assertion evidence source_evidence_literature NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_assertion SIO_000772 11745996 NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_assertion wasDerivedFrom befree-20140225 NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_assertion wasGeneratedBy ECO_0000203 NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP355419.RA_RNNq2ZKV6Izi0C5iqhoqe9lOWimgfxx1HJ5XH7ltpk130_provenance.