Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_assertion> ?p ?o ?g. }
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- NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_assertion type Assertion NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_head.
- NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_assertion description "[Some ovarian fibromas and rare fibrosarcomas are associated with Gorlin syndrome, which is caused by mutation in the human homologue of Drosophila patched gene (PTCH), localized on chromosome 9q22.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_provenance.
- NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_assertion evidence source_evidence_literature NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_provenance.
- NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_assertion SIO_000772 16084949 NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_provenance.
- NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_assertion wasDerivedFrom befree-20140225 NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_provenance.
- NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_assertion wasGeneratedBy ECO_0000203 NP176798.RA0Z1dZkL2CpwHYPB7NM6WRlTi2pyrfktmU7mId6zdu-0130_provenance.