Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_assertion description "[Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_assertion evidence source_evidence_literature NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_assertion SIO_000772 17767372 NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_assertion wasDerivedFrom befree-2016 NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_assertion wasGeneratedBy ECO_0000203 NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.
- befree-2016 importedOn "2016-02-19" NP627917.RAI72O7Yz3O13aElKoeYk1WYOeDPRUnPBQ2wsdv9iCXRk130_provenance.