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- source_evidence_literature type ECO_0000212 NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_assertion description "[The conclusion that most variants of OI are caused by mutations in the structural genes for type I procollagen has broad implications for other diseases that affect connective tissue, diseases such as chondrodystrophies, osteoarthritis, and osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_assertion evidence source_evidence_literature NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_assertion SIO_000772 2683782 NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_assertion wasDerivedFrom befree-2016 NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_assertion wasGeneratedBy ECO_0000203 NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296073.RANRXsZrlArIMXrlQYswTOIW92-6zK-Tvopwp8uf2w51g130_provenance.