Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_assertion description "[Twenty percent of CIN III and 41% of InCa had patterns compatible with Ha-ras mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_assertion evidence source_evidence_literature NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_assertion SIO_000772 12878090 NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_assertion wasDerivedFrom befree-20140225 NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_assertion wasGeneratedBy ECO_0000203 NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP309232.RAF79g4rDOu3Ah973LWvbmGxpfC1OU5Ax2hifS8U7XA8M130_provenance.