Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_assertion> ?p ?o ?g. }
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- NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_assertion type Assertion NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_head.
- NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_assertion wasGeneratedBy ECO_0000203 NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_provenance.
- NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_assertion wasDerivedFrom befree-20140225 NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_provenance.
- NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_assertion SIO_000772 16505158 NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_provenance.
- NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_assertion evidence source_evidence_literature NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_provenance.
- NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_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." NP377387.RATJX040RRIeirnEW4vGCiENRrcxUirPEiRbI-ivGJUHw130_provenance.