Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_assertion description "[While NBS shares overlapping characteristics with ataxia telangiectasia, it also has features overlapping with ATR-Seckel (ATR: ataxia-telangiectasia and Rad3-related protein) syndrome, a subclass of Seckel syndrome mutated in ATR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_assertion evidence source_evidence_literature NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_assertion SIO_000772 15616588 NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_assertion wasDerivedFrom befree-20140225 NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_assertion wasGeneratedBy ECO_0000203 NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212994.RASgCeizR1_T3U39zqyrKxnr-zJk3J_V4amI13MjuMuFQ130_provenance.