Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_assertion type Assertion NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_head.
- NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_assertion description "[Clinical findings are different in 9q deletions and duplications including PTCH1, notably concerning the predisposition to benign and malignant tumors reported in the Gorlin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.
- NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_assertion evidence source_evidence_literature NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.
- NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_assertion SIO_000772 24486987 NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.
- NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_assertion wasDerivedFrom befree-2016 NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.
- NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_assertion wasGeneratedBy ECO_0000203 NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.