Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_assertion type Assertion NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_head.
- NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_assertion wasGeneratedBy ECO_0000203 NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_provenance.
- NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_assertion wasDerivedFrom gad-20150221 NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_provenance.
- NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_assertion SIO_000772 19657220 NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_provenance.
- NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_assertion evidence source_evidence_literature NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_provenance.
- NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_assertion description "[The percentage of N29I mutations in ACP patients was higher than that reported in other studies, while the percentage of N34S and AAT mutations in ACP and idiopathic CP patients was similar.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87950.RArArYvMQvU9Xzw68uzuvW4x8Vx_UHn4q-Wup5lXw7VQI130_provenance.