Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_assertion description "[Results describe a series of new mutations in the OCA genes, and their role in the molecular diagnosis of oculocutaneous albinism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_assertion evidence source_evidence_literature NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_assertion SIO_000772 18821858 NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_assertion wasDerivedFrom lhgdn-20090331 NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_assertion wasGeneratedBy ECO_0000203 NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215657.RAM0KPDoxgwPClxAXLckK57MQd-UEyopxLLyVdm-lXfwc130_provenance.