Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_assertion description "[GLRB itself does not seem to be a good candidate as it causes autosomal recessive hyperekplexia and no symptoms were found in the patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_assertion evidence source_evidence_literature NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_assertion SIO_000772 22669415 NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_assertion wasDerivedFrom befree-20140225 NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_assertion wasGeneratedBy ECO_0000203 NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP277558.RAwgWmYkcfxe83TIHNipWkK7LB6SX7IKBvpy45j46zRrg130_provenance.