Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- befree-2016 importedOn "2016-02-19" NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_assertion wasGeneratedBy ECO_0000203 NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_assertion wasDerivedFrom befree-2016 NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_assertion SIO_000772 16332960 NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_assertion evidence source_evidence_literature NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.
- NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_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." NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.