Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_assertion description "[We analysed 3D facial photographs of 51 males and 15 females with full FMR1 mutations and 9 females with a premutation using dense-surface modelling techniques and a new technique that forms a directed graph with normalized face shapes as nodes and edges linking those with closest dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_assertion evidence source_evidence_literature NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_assertion SIO_000772 23211703 NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_assertion wasDerivedFrom befree-20150227 NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_assertion wasGeneratedBy ECO_0000203 NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412732.RA2QjHENnMO_fc-b13XZV0ovG4yr-api8kt2m8QndVlzE130_provenance.