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- source_evidence_literature type ECO_0000212 NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_assertion description "[While the noggin gene (NOG) is not mutated in patients who have FOP, these findings extend a growing body of evidence implicating overactivity of the BMP signaling pathway in the molecular pathogenesis of FOP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_assertion evidence source_evidence_literature NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_assertion SIO_000772 15959366 NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_assertion wasDerivedFrom befree-20140225 NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_assertion wasGeneratedBy ECO_0000203 NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP812880.RA4zIULlOJh6HGm4UlewEJNDbXqsbf1h6u1Hlfw6DmUYc130_provenance.