Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_assertion description "[The phenotypic correlation with the mouse Herc1 and Herc2 mutants as well as the phenotypic overlap with Angelman syndrome provide further evidence that pathogenic changes in HERC2 are associated with nonsyndromic intellectual disability, autism, and gait disturbance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_assertion evidence source_evidence_literature NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_assertion SIO_000772 23065719 NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_assertion wasDerivedFrom befree-20140225 NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_assertion wasGeneratedBy ECO_0000203 NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651233.RAuYUd8bmRLD_ZBv7SIRdLe8lsWw49IRVEaIqPAGO9PE0130_provenance.