Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_assertion> ?p ?o ?g. }
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- NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_assertion type Assertion NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_head.
- NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_assertion description "[The human molybdenum cofactor sulfurase (HMCS) gene, the human ma-l homologue, is therefore a candidate gene responsible for classical xanthinuria type II, which involves both XDH and AO deficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_provenance.
- NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_assertion evidence source_evidence_literature NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_provenance.
- NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_assertion SIO_000772 11302742 NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_provenance.
- NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_assertion wasDerivedFrom befree-20140225 NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_provenance.
- NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_assertion wasGeneratedBy ECO_0000203 NP836304.RAMBboU2ogWXFfQA6U-lYNiz7HyS-Lr_VaT_7yhiw-Z8o130_provenance.