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- source_evidence_literature type ECO_0000212 NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- befree-20150227 importedOn "2015-02-27" NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_assertion wasGeneratedBy ECO_0000203 NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_assertion wasDerivedFrom befree-20150227 NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_assertion SIO_000772 21236492 NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_assertion evidence source_evidence_literature NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.
- NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_assertion description "[To describe a novel laminin β-2 (LAMB2) mutation associated with nephrotic syndrome and severe retinal disease without microcoria in a large, multigenerational family with Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958115.RAlxvbe74ZX-jwIHLxNxMAJmgOvA-MW810QoY_3fHc6Js130_provenance.