Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_assertion description "[Missense mutations in the BCS1L gene as a cause of the Bjrnstad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_assertion evidence source_evidence_curated NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_assertion SIO_000772 17314340 NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_assertion wasDerivedFrom uniprot-20130724 NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_assertion wasGeneratedBy ECO_0000218 NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP715.RAFWtdULTJnDgrwV11tU_v1KxvQUTyy_qRMZOROEErQFs130_provenance.