Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_assertion wasGeneratedBy ECO_0000203 NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_assertion wasDerivedFrom befree-20150227 NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_assertion SIO_000772 16332960 NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_assertion evidence source_evidence_literature NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.