Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_assertion description "[Mutations in FA2H are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_assertion evidence source_evidence_literature NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_assertion SIO_000772 19068277 NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_assertion wasDerivedFrom lhgdn-20090331 NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_assertion wasGeneratedBy ECO_0000203 NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP140761.RAuKUND2kD5w1c8zRZzFtGa24693SI75frE2Fb9XmVMWw130_provenance.