Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_assertion description "[Mutations in the crumbs homologue 1 (CRB1) gene cause a specific form of retinitis pigmentosa (RP) that is designated RP12 and is characterized by a preserved para-arteriolar retinal pigment epithelium (PPRPE) and by severe loss of vision at age <20 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_assertion evidence source_evidence_literature NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_assertion SIO_000772 11389483 NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_assertion wasDerivedFrom befree-2016 NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_assertion wasGeneratedBy ECO_0000203 NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.
- befree-2016 importedOn "2016-02-19" NP319837.RAK7mXL2GuVe4HRHaAiinKPpoO3vPbcmev3fYfy47Pv1U130_provenance.