Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_assertion description "[Patients were classified according to age of onset, clinical pattern, and associated neurological signs into `ULD-like` and `not ULD-like.` After exclusion of mutations in cystatin B (CSTB), DNA was examined for sequence variation in SCARB2 and PRICKLE1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_assertion evidence source_evidence_literature NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_assertion SIO_000772 19847901 NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_assertion wasDerivedFrom befree-20140225 NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_assertion wasGeneratedBy ECO_0000203 NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP605355.RA4aRcTs4JgQhi2SFJmwfuYc0uY_CNqSD2OeOvlgLYZ_0130_provenance.