Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_assertion description "[ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_assertion evidence source_evidence_literature NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_assertion SIO_000772 21204215 NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_assertion wasDerivedFrom befree-2016 NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_assertion wasGeneratedBy ECO_0000203 NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.
- befree-2016 importedOn "2016-02-19" NP862850.RA-xmaC3DvU42L42h9CeTXl5vDs2KBxWeiHDRxJGj6OC8130_provenance.