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- source_evidence_literature type ECO_0000212 NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_assertion description "[Therefore, on one hand our data confirm a role of driver mutations for copy number alterations (CNAs) included in the GBM genomic-signature (gain of chromosome 7- EGFR gene, loss of chromosome 13- RB1 gene, loss of chromosome 10-PTEN gene); on the other, it is not obvious that the new identified CNAs are passenger mutations, as they may be necessary for tumor progression specific for the individual patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_assertion evidence source_evidence_literature NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_assertion SIO_000772 23468990 NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_assertion wasDerivedFrom befree-20150227 NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_assertion wasGeneratedBy ECO_0000203 NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP654342.RAXIq8linIQLG7xkMRK6fh1eMFUMmGZXmnDbrTYn15Sm0130_provenance.