Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_assertion> ?p ?o ?g. }
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- NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_assertion type Assertion NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_head.
- NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_assertion wasGeneratedBy ECO_0000203 NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_provenance.
- NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_assertion wasDerivedFrom befree-20140225 NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_provenance.
- NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_assertion SIO_000772 11702207 NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_provenance.
- NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_assertion evidence source_evidence_literature NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_provenance.
- NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_assertion description "[Retinitis pigmentosa 3 (RP3) is a progressive retinal degeneration due to mutations in the X-linked RPGR gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181078.RARxL2WG5QlUeLfjMY7OWdKPZMmWj-GLdovykcqcEwIAE130_provenance.