Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_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." NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_assertion evidence source_evidence_literature NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_assertion SIO_000772 19847901 NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_assertion wasDerivedFrom befree-2016 NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_assertion wasGeneratedBy ECO_0000203 NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.
- befree-2016 importedOn "2016-02-19" NP771017.RAQ_aq1fejVRU5BiRWScXZG3F71iV7BvxLGMU0r7fks2M130_provenance.