Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_assertion description "[The data suggest that different COL17A1 mutations and their combinations can result in a spectrum of biologic and clinical phenotypes of not only generalized atrophic benign epidermolysis bullosa, but also localized junctional epidermolysis bullosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_assertion evidence source_evidence_literature NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_assertion SIO_000772 9740252 NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_assertion wasDerivedFrom befree-20150227 NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_assertion wasGeneratedBy ECO_0000203 NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP321243.RAUaWI5tN9Y-6pkTRbZQ-P_4XkkT7oM_5HXVxinpT_qsI130_provenance.