Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_assertion wasGeneratedBy ECO_0000203 NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_assertion wasDerivedFrom befree-20140225 NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_assertion SIO_000772 8028668 NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_assertion evidence source_evidence_literature NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_assertion description "[Sequence analysis revealed a striking identity (99%) of the subunit with a protein encoded by the causative gene (LIS-1) for Miller-Dieker lissencephaly, a human brain malformation manifested by a smooth cerebral surface and abnormal neuronal migration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP448553.RAJCLBXU0fNXeNSWGeJ6WQjzUhz5fYRAQEtEOjJkuPT1s130_provenance.