Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_assertion type Assertion NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_head.
- NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_assertion wasGeneratedBy ECO_0000218 NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_provenance.
- NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_assertion wasDerivedFrom uniprot-2016 NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_provenance.
- NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_assertion SIO_000772 8871668 NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_provenance.
- NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_assertion evidence source_evidence_curated NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_provenance.
- NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_assertion description "[Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9185.RABuNb2wKIsmR97fcSKPPTzOgValGjL5BfNuED1f8BwLc130_provenance.