Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion> ?p ?o ?g. }
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- NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion type Assertion NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_head.
- NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_provenance.
- NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion evidence source_evidence_literature NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_provenance.
- NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion SIO_000772 22236406 NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_provenance.
- NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion wasDerivedFrom befree-20150227 NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_provenance.
- NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion wasGeneratedBy ECO_0000203 NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_provenance.