Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_assertion description "[The results indicate that (1) LOH at both PTCH gene and STK11 gene is relatively frequent in cellular fibromas; (2) approximately a quarter of luteinized thecomas exhibited LOH of the PTCH gene; in both neoplasms, cellular fibromas and luteinized thecomas, LOH may play a role in their pathogenesis; and (3) sporadic cellular fibromas may arise through similar genetic pathways as cases of Gorlin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_assertion evidence source_evidence_literature NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_assertion SIO_000772 16084949 NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_assertion wasDerivedFrom befree-20150227 NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_assertion wasGeneratedBy ECO_0000203 NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP653322.RAuzgUMhCIae98a9P_NnCWZcHhnnUhRt1uASyCYCk--dI130_provenance.