Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion evidence source_evidence_curated NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion SIO_000772 11030761 NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion wasDerivedFrom uniprot-20150221 NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion wasGeneratedBy ECO_0000218 NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.