Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_assertion description "[This study confirms that TULP1 mutations cause a severe early-onset form of autosomal recessive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_assertion evidence source_evidence_literature NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_assertion SIO_000772 17620573 NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_assertion wasDerivedFrom befree-2016 NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_assertion wasGeneratedBy ECO_0000203 NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.
- befree-2016 importedOn "2016-02-19" NP619283.RA3QQqqezeGv3O1tK3JlqZKBSLcAmUmgJpiWWisbuXYmI130_provenance.