Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_assertion> ?p ?o ?g. }
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- NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_assertion type Assertion NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_head.
- NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_assertion wasGeneratedBy ECO_0000218 NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_provenance.
- NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_assertion wasDerivedFrom uniprot-20130724 NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_provenance.
- NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_assertion SIO_000772 15346351 NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_provenance.
- NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_assertion evidence source_evidence_curated NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_provenance.
- NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_assertion description "[Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3868.RASo5cLZGOKjNw_kmrrxhXIxICeumvBO0xiAJ2rSinWBY130_provenance.