Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_assertion> ?p ?o ?g. }
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- NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_assertion type Assertion NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_head.
- NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_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." NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_provenance.
- NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_assertion evidence source_evidence_literature NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_provenance.
- NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_assertion SIO_000772 19847901 NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_provenance.
- NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_assertion wasDerivedFrom befree-20150227 NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_provenance.
- NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_assertion wasGeneratedBy ECO_0000203 NP974025.RAxnxwZi-cRQuBPYXsHliAL-LqXMEw5yBSuV6481vXZfs130_provenance.