Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_assertion description "[Herein are illustrated some pitfalls in the diagnosis of melanoma, as well as variants of Spitz's nevus that correlate with specific genomic aberrations such as gains of chromosome 11p and loss of the BAP-1 gene on chromosome 3p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_assertion evidence source_evidence_literature NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_assertion SIO_000772 22648325 NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_assertion wasDerivedFrom befree-20150227 NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_assertion wasGeneratedBy ECO_0000203 NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP818134.RAEj8H3vK21Ke4cjV6bxX7xrt2Yji3gg6ZCMtbMfwtRpQ130_provenance.