Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_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." NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion evidence source_evidence_literature NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion SIO_000772 10480362 NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion wasDerivedFrom befree-20150227 NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion wasGeneratedBy ECO_0000203 NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.