Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_assertion description "[Mutation analysis of LIS1, using highly sensitive techniques such as denaturing high-pressure liquid chromatography, should be considered for patients with posteriorly predominant subcortical band heterotopia and pachygyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_assertion evidence source_evidence_literature NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_assertion SIO_000772 14581661 NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_assertion wasDerivedFrom befree-20140225 NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_assertion wasGeneratedBy ECO_0000203 NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP882209.RA_UG-tF8pFK8-xxPG2M0ydJkadYePBLlqmvXJdNXuxB0130_provenance.