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- source_evidence_literature type ECO_0000212 NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_assertion description "[HMSN type II (HMSN II) or CMT2, the axonal form of CMT, is genetically heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_assertion evidence source_evidence_literature NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_assertion SIO_000772 9595994 NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_assertion wasDerivedFrom befree-2016 NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_assertion wasGeneratedBy ECO_0000203 NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1395623.RAuu8oB3R7Dx7GUysTJbOoQAo-60BJ_X_m8p-OxuB7sdM130_provenance.