Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_assertion description "[It is noteworthy that contrary to a previous study, we did not find an association between the MMP9 (nt-1562) polymorphism and AAA, suggesting genetic heterogeneity of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_assertion evidence source_evidence_literature NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_assertion SIO_000772 15944607 NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_assertion wasDerivedFrom befree-20140225 NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_assertion wasGeneratedBy ECO_0000203 NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP766624.RAskP675jYsri4kuPHbNVHyA_PCiw7I33PKiYIf-nqW6w130_provenance.