Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP512658.RAW2hX_MQxhuqLaBUP8DgM2zdQA7GvM1izmV1kqUWUxto130_provenance.