Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_assertion description "[It is conceivable that germline sequence variation in other BER pathway genes such as NTHL1, NEIL1, NEIL2, MPG, TDG, UNG and SMUG1 also contribute to CRC susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_assertion evidence source_evidence_literature NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_assertion SIO_000772 17029639 NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_assertion wasDerivedFrom befree-20140225 NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_assertion wasGeneratedBy ECO_0000203 NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP557676.RAqM8aEzpnm0SPJATl9_Pq5iff9hfly9suZb3XL_oJ5Hs130_provenance.