Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_assertion description "[We detected a 22q11 deletion in a patient with moderate MR, obesity, and facial dysmorphism and a 4 Mb 17p11 duplication in a patient with moderate MR, behaviour disturbance, strabismus, and aspecific facial features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_assertion evidence source_evidence_literature NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_assertion SIO_000772 16773131 NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_assertion wasDerivedFrom befree-20140225 NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_assertion wasGeneratedBy ECO_0000203 NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP589488.RAgVByZM5g8yTdjxM4Cj0ESiCjBfwfF6ETDjjy0Uf2-_k130_provenance.