Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_assertion description "[We also performed a full genome screen for chromosomal abnormalities, and searched for mutations in two genes (GPR143 and OCA2) known to be associated with ocular albinism and PAX6 gene known to be associated with aniridia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_assertion evidence source_evidence_literature NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_assertion SIO_000772 21264491 NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_assertion wasDerivedFrom befree-20140225 NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_assertion wasGeneratedBy ECO_0000203 NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP639428.RAFMrzt3MQwcx8EL-bY_b18VO4uzkOXECXY11W8lsTWCE130_provenance.