Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion wasGeneratedBy ECO_0000203 NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion wasDerivedFrom befree-2016 NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion SIO_000772 8037181 NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion evidence source_evidence_literature NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.
- NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion description "[In the present report, we extend our analysis of p53 gene mutations to 70 cases of AML representative of the other FAB types of the disease, including M1 (16 cases), M2 (20 cases), M4 (17 cases), M5 (12 cases), and M6 (5 cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance.