Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_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." NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_assertion evidence source_evidence_literature NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_assertion SIO_000772 17767372 NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_assertion wasDerivedFrom befree-20140225 NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_assertion wasGeneratedBy ECO_0000203 NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775099.RAW2LPSWqLPxBs7D58gJbdeap_smZ0SarTlbnR9_uERlU130_provenance.