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- source_evidence_literature type ECO_0000212 NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_assertion evidence source_evidence_literature NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_assertion SIO_000772 24676634 NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_assertion wasDerivedFrom befree-2016 NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_assertion wasGeneratedBy ECO_0000203 NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.
- befree-2016 importedOn "2016-02-19" NP1168179.RA51SLMX-IQC6Wo0QZFfgSEVUo8jgnAtim9qjJuP_7j38130_provenance.