Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_assertion description "[HNF1B gene anomalies include renal development defects associated with cysts and are well known by pediatric nephrologists that ask for molecular analysis of this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_assertion evidence source_evidence_literature NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_assertion SIO_000772 23261960 NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_assertion wasDerivedFrom befree-20150227 NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_assertion wasGeneratedBy ECO_0000203 NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724973.RASn8RnxOx6-sxTcapGU2a5cNS-HAmiIqGtlfyryIShcI130_provenance.