Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_assertion description "[Mutations of the p53 gene were found in two cases, at codon 244 (GGC to TGC) in the cholangiocellular carcinoma component of case 1 (mixed type, showing an intimate intermingling of both elements) and at codon 234 (TAC to AAC) in both components of case 5 (combined type, consisting of contiguous but independent masses of both elements).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_assertion evidence source_evidence_literature NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_assertion SIO_000772 8957064 NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_assertion wasDerivedFrom befree-2016 NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_assertion wasGeneratedBy ECO_0000203 NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1364009.RAGQX5qKCfNidQIs0bQAvGySHHcQ95TlJR4AqeGJ8JMnk130_provenance.