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- source_evidence_literature type ECO_0000212 NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_assertion description "[However, electroclinical descriptions in patients with ISSX carrying ARX mutations are scarce.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_assertion evidence source_evidence_literature NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_assertion SIO_000772 18468866 NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_assertion wasDerivedFrom befree-20150227 NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_assertion wasGeneratedBy ECO_0000203 NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978213.RAFJIItjqzLbBAlpDt5w7PGzp4f_h16pz0ZDPuz6Cyo5s130_provenance.