Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_assertion type Assertion NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_head.
- NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_assertion description "[Sanfilippo syndrome type B (mucopolysaccharidosis IIIB) is an autosomal recessive disease that is caused by the deficiency of the lysosomal enzyme alpha-N-acetylglucosaminidase (NAGLU).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.
- NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_assertion evidence source_evidence_literature NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.
- NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_assertion SIO_000772 16151907 NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.
- NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_assertion wasDerivedFrom befree-2016 NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.
- NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_assertion wasGeneratedBy ECO_0000203 NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.