Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_assertion description "[Dopa-responsive dystonia (DRD) is an autosomal-dominant neurological disorder which appears to result from a genetically determined deficiency of striatal dopamine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_assertion evidence source_evidence_literature NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_assertion SIO_000772 8298648 NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_assertion wasDerivedFrom befree-20140225 NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_assertion wasGeneratedBy ECO_0000203 NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP630528.RA4pTc3UCjwyUXLWgSiJAkXgkBSHzaZrzDfsyKPAM4PbU130_provenance.