Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_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." NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_assertion evidence source_evidence_literature NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_assertion SIO_000772 10480362 NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_assertion wasDerivedFrom befree-20150227 NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_assertion wasGeneratedBy ECO_0000203 NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP800402.RAQ8VY2A0RjpoOdd3nV2ue-KLmIPfkiWOhPdbNxmCeTxo130_provenance.