Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- befree-2016 importedOn "2016-02-19" NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion wasGeneratedBy ECO_0000203 NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion wasDerivedFrom befree-2016 NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion SIO_000772 22152678 NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion evidence source_evidence_literature NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion description "[We used whole-exome sequencing of five unrelated individuals with lepto-SEMDJL to identify mutations in KIF22 as the cause of this skeletal condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.