Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_assertion description "[Differences in mutation profiles and patterns of gene gains/losses are seen between BRCA2 (associated with TP53/PTEN mutations, loss of RB1 and gain of HRAS, STK11 and SMARCB1) and BRCAX (associated with PIK3CA mutations) tumours, suggesting that BRCA2 and BRCAX MBCs may be distinct and arise from different tumour pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_assertion evidence source_evidence_literature NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_assertion SIO_000772 25490678 NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_assertion wasDerivedFrom befree-2016 NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_assertion wasGeneratedBy ECO_0000203 NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246469.RAF9Wz7Ab9KhnTz2xjxO2bbP00K8awZtMfxJwitylzIVc130_provenance.