Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_assertion description "[The BRCA1 and BRCA2 genes from the MBC patients were screened for four highly recurrent mutations in the Slovenian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_assertion evidence source_evidence_literature NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_assertion SIO_000772 18439106 NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_assertion wasDerivedFrom befree-2016 NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_assertion wasGeneratedBy ECO_0000203 NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.
- befree-2016 importedOn "2016-02-19" NP668038.RAc3vvOwClciIWNFsBEFFUKvucEB5H1vVfqwYy6rfKKXI130_provenance.