Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_assertion wasGeneratedBy ECO_0000203 NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_assertion wasDerivedFrom befree-20140225 NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_assertion SIO_000772 16505158 NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_assertion evidence source_evidence_literature NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP381516.RA6Es8b-ij2lU-2GuM2UZK_HE2VvX2tsZtERvApzVAJPI130_provenance.