Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_assertion description "[In addition, cerebellar hypoplasia and Walcott-Rallison syndrome have been associated with PNDM, suggesting an autosomal recessive inheritance pattern; furthermore, a mutation in the gene insulin promoter factor 1 has been identified as a cause of pancreatic agenesis in PNDM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_assertion evidence source_evidence_literature NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_assertion SIO_000772 10895036 NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_assertion wasDerivedFrom befree-20140225 NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_assertion wasGeneratedBy ECO_0000203 NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.