Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_assertion description "[We sequenced C5orf42 in 313 JS probands and identified mutations in 28 (8.9�%), most with a phenotype of pure JS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_assertion evidence source_evidence_literature NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_assertion SIO_000772 25407461 NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_assertion wasDerivedFrom befree-2016 NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_assertion wasGeneratedBy ECO_0000203 NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238415.RA1R_3h9W8QKVy0zm7V2i_pZ9mm_Oew0Uh3mfFntuYEgU130_provenance.