Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_assertion description "[Lissencephaly caused by LIS1 or DCX mutation frequently results in West syndrome, while lissencephaly due to ARX mutation is associated with the most severe form of epilepsy but never results in West syndrome nor infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_assertion evidence source_evidence_literature NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_assertion SIO_000772 16806828 NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_assertion wasDerivedFrom befree-20150227 NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_assertion wasGeneratedBy ECO_0000203 NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP605905.RA8cpiVSKfhvXzvi_Pwha_EAUIqCrSLzK7ChI4XgWzudw130_provenance.