Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_assertion wasGeneratedBy ECO_0000203 NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_assertion wasDerivedFrom befree-20140225 NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_assertion SIO_000772 10982035 NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_assertion evidence source_evidence_literature NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_assertion description "[This novel approach identified an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three cases of unexplained mental retardation and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP249222.RAdHFQWj4z1ArrnipmG1x7lghKtgD8m8NFBv3M0BQ7CJA130_provenance.