Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1151170.RAUGjPVIP4t7osdwNJxld0aEpNw6TgdLEQpHTKByHiX_E130_provenance.