Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_assertion description "[A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_assertion evidence source_evidence_literature NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_assertion SIO_000772 9810570 NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_assertion wasDerivedFrom befree-20140225 NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_assertion wasGeneratedBy ECO_0000203 NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP888118.RA_l3xHdbm5pIka7ZRlssU8l419nFhuk07XoBPc2hsnpk130_provenance.