Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_assertion description "[(2) The human homolog of int-2, located on chromosome 11q13, is frequently amplified in human primary tumors and is comprised in an amplification unit encompassing the hst gene, which is often coamplified; the amplification at the 11q13 locus in breast carcinomas correlates with a poor outcome of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_assertion evidence source_evidence_literature NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_assertion SIO_000772 2677918 NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_assertion wasDerivedFrom befree-2016 NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_assertion wasGeneratedBy ECO_0000203 NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295978.RAZGEKaVD_oJ0WWazez1DzuJsawJsezQf5_CSe5xpQNkI130_provenance.