Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_assertion wasGeneratedBy ECO_0000203 NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_assertion wasDerivedFrom befree-2016 NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_assertion SIO_000772 8028668 NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_assertion evidence source_evidence_literature NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.
- NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_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." NP1330268.RAXFAOiYMtrte_dgRUpOe-UHwWE0JmBwgH5NRXWVhjQfQ130_provenance.