Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_assertion description "[The autosomal dominant form of familial neurohypophyseal diabetes insipidus (adFNDI) has been linked to 40 different mutations of the gene encoding the vasopressin-neurophysin II (AVP-NPII) precursor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_assertion evidence source_evidence_curated NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_assertion SIO_000772 12107248 NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_assertion wasDerivedFrom uniprot-20130724 NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_assertion wasGeneratedBy ECO_0000218 NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP639.RAg_kHbLhJbYHv120Ho74FbPj9tMBh0fXr0O6cTw__mJE130_provenance.