Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_assertion description "[A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_assertion evidence source_evidence_literature NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_assertion SIO_000772 16080123 NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_assertion wasDerivedFrom befree-2016 NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_assertion wasGeneratedBy ECO_0000203 NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP507370.RAOJTx9ovXX4wSXHmysrB3a40Fzn6Mg4BPGUnlJdR6W_Q130_provenance.