Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_assertion> ?p ?o ?g. }
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- NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_assertion type Assertion NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_head.
- NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_assertion description "[The retinal dystrophy associated with the Pro23Ala mutation is characteristically mild in presentation and course, with greater preservation of ERG amplitudes than the more prevalent Pro23His mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_provenance.
- NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_assertion evidence source_evidence_literature NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_provenance.
- NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_assertion SIO_000772 10980774 NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_provenance.
- NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_assertion wasDerivedFrom befree-20140225 NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_provenance.
- NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_assertion wasGeneratedBy ECO_0000203 NP925375.RAo9V4moo6Drn0A6M8r7tXk9goNla6NVKb7ZvfsKchGQA130_provenance.