Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- befree-2016 importedOn "2016-02-19" NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_assertion wasGeneratedBy ECO_0000203 NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_assertion wasDerivedFrom befree-2016 NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_assertion SIO_000772 20332263 NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_assertion evidence source_evidence_literature NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.
- NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_assertion description "[We genotyped the 10 most statistically significant loci (most significant single-nucleotide polymorphism located in ARHGAP10; P = 2.28 x 10(-7)) in 4,335 women diagnosed with invasive breast cancer (38,148 years at risk) in the SEARCH (Studies of Epidemiology and Risk factors in Cancer Heredity) breast cancer study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801955.RAujpMWx6q7h03bpcbsfAjQuz13gmtA7WwYHKAR2BrVpI130_provenance.