Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_assertion description "[Gene sequencing failed to reveal PLA2G6 mutations, indicating that fetal neuroaxonal dystrophy presenting as fetal akinesia deformation sequence is genetically distinct from infantile neuroaxonal dystrophy and related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_assertion evidence source_evidence_literature NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_assertion SIO_000772 20235854 NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_assertion wasDerivedFrom befree-2016 NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_assertion wasGeneratedBy ECO_0000203 NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.
- befree-2016 importedOn "2016-02-19" NP800462.RAXCDewV5C_DAeLcpPBaVlLzRk__vbuOo8jO8c1-343k4130_provenance.