Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_assertion description "[We suggest that mutations such as this one may disrupt EGF-like domain folding less drastically than do substitutions of cysteine or of other amino acids important for calcium-binding that cause classical MFS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_assertion evidence source_evidence_literature NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_assertion SIO_000772 7762551 NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_assertion wasDerivedFrom befree-2016 NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_assertion wasGeneratedBy ECO_0000203 NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1321088.RA4FOTvI8nuhY2BOsuMD3qNztWufv3-xSpfK9xNDYMRbo130_provenance.