Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_assertion description "[Both patients presented with neonatal diabetes mellitus, severe resistant hypothyroidism in the presence of elevated thyroglobulin and normal thyroid anatomy, degenerative liver disease, cystic renal dysplasia, recurrent infections and facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_assertion evidence source_evidence_literature NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_assertion SIO_000772 21139041 NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_assertion wasDerivedFrom befree-20140225 NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_assertion wasGeneratedBy ECO_0000203 NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP846729.RA4cQV7D2MR1etV3wTxWS4wLxGzF93mZ1PXjNIXd1PtMI130_provenance.