Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_assertion description "[Autosomal recessive forms of infantile dystonia due to mutations in the tyrosine hydroxylase (TH) gene have been described recently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_assertion evidence source_evidence_literature NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_assertion SIO_000772 15747353 NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_assertion wasDerivedFrom befree-2016 NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_assertion wasGeneratedBy ECO_0000203 NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.
- befree-2016 importedOn "2016-02-19" NP483886.RA7BH31WorI0sUHiObS8vdqOO-8vxsQEtDq0a0kImtF_o130_provenance.