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- source_evidence_literature type ECO_0000212 NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_assertion evidence source_evidence_literature NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_assertion SIO_000772 22532172 NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_assertion wasDerivedFrom befree-2016 NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_assertion wasGeneratedBy ECO_0000203 NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- befree-2016 importedOn "2016-02-19" NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.