Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_assertion type Assertion NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_head.
- NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_assertion wasGeneratedBy ECO_0000218 NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_provenance.
- NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_assertion wasDerivedFrom ctd_human-20130708 NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_provenance.
- NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_assertion SIO_000772 15146389 NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_provenance.
- NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_assertion evidence source_evidence_curated NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_provenance.
- NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_assertion description "[A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18283.RAJIoJex32FNMYTwjY66orgyL-cqUa1d9LH3ZplZXb5yw130_provenance.