Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_assertion description "[We sought to determine the proportion of non-founder mutations as a percentage of all mutations in BRCA1 and BRCA2 among AJ patients to inform decisions about HBOC testing strategies in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_assertion evidence source_evidence_literature NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_assertion SIO_000772 25476495 NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_assertion wasDerivedFrom befree-2016 NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_assertion wasGeneratedBy ECO_0000203 NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244943.RAaUuGnJDWygDB3Qk9wCfvn8tdzSAEYzPyqsKG5wMycfE130_provenance.