Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_assertion wasGeneratedBy ECO_0000203 NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_assertion wasDerivedFrom befree-20140225 NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_assertion SIO_000772 16753021 NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_assertion evidence source_evidence_literature NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_assertion description "[Whereas the primary genetic defect in this condition is unknown, BMP4 mRNA and protein and BMP receptor type IA (BMPRIA) protein are overexpressed in cultured lymphocytes from FOP patients, supporting that altered BMP signaling is involved in this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP578940.RApc1BlmE8qcBuTBG7pD6ySWOES7z8Yxc_HCm1xRG0axA130_provenance.