Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_assertion description "[We considered that the CHRD gene and the chordin-regulating GSC (goosecoid) gene could be candidate genes for Cornelia de Lange syndrome (CDLS), a developmental malformation syndrome which is primarily characterised by mental handicap, growth retardation, distinctive facial features and limb-reduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_assertion evidence source_evidence_literature NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_assertion SIO_000772 10480362 NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_assertion wasDerivedFrom befree-20140225 NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_assertion wasGeneratedBy ECO_0000203 NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.
- befree-20140225 importedOn "2014-02-25" NP169082.RAR4x99EEMz3WWVztRn1rtrAnXfOXyv6L0EdklL1Teu44130_provenance.