Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion> ?p ?o ?g. }
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- NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion type Assertion NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_head.
- NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion wasGeneratedBy ECO_0000218 NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_provenance.
- NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion wasDerivedFrom uniprot-20130724 NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_provenance.
- NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion SIO_000772 8318557 NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_provenance.
- NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion evidence source_evidence_curated NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_provenance.
- NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion description "[Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_provenance.