Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_assertion description "[Thus, it illustrates the need to include p14(ARF)- and p16(INK4a) transcript analysis when searching for unknown mutations within the CDKN2A locus in melanoma-prone families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_assertion evidence source_evidence_literature NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_assertion SIO_000772 17001621 NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_assertion wasDerivedFrom befree-20140225 NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_assertion wasGeneratedBy ECO_0000203 NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP743936.RAHM6XsMqvGWqsHMJNqpThyfNwrp2kIjfHdGOBH-19bdg130_provenance.