Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_assertion wasGeneratedBy ECO_0000218 NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_assertion wasDerivedFrom uniprot-20130724 NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_assertion SIO_000772 14624414 NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_assertion evidence source_evidence_curated NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_assertion description "[Identification of a new point mutation in the human molybdenum cofactor sulferase gene that is responsible for xanthinuria type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4091.RATYWh2JjbRz-aJ5Q2YjUBsPfwLiC168kJJWrG2dj-32M130_provenance.