Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_assertion description "[CS clinical features, including developmental delay, the typical facial gestalt, chorioretinal dystrophy (CRD) and neutropenia, are well described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_assertion evidence source_evidence_literature NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_assertion SIO_000772 23188044 NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_assertion wasDerivedFrom befree-20140225 NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_assertion wasGeneratedBy ECO_0000203 NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP300541.RAIx9UMk5PiySw1L8948WdnrEUpoxYQ4_O6COkXAmkTi0130_provenance.