Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_assertion description "[The Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI) is a lysosomal storage disease with autosomal recessive inheritance caused by deficiency of the enzyme arylsulfatase B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_assertion evidence source_evidence_literature NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_assertion SIO_000772 1718978 NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_assertion wasDerivedFrom befree-2016 NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_assertion wasGeneratedBy ECO_0000203 NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.
- befree-2016 importedOn "2016-02-19" NP586119.RAe1b4tlFEl8KBVmB8Xqfnv2EQNFy8msfg2grEw0zfics130_provenance.