Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_assertion description "[The results demonstrate that patients with cGVHD had a higher incidence of HP 2-2 phenotype (43.8%), in comparison to the patients without cGVHD (0%) and normal donors (18.7%), suggesting the possibility that specific Hp polymorphism may play a role in the development of cGVHD after allo-HCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_assertion evidence source_evidence_literature NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_assertion SIO_000772 19379511 NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_assertion wasDerivedFrom befree-20150227 NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_assertion wasGeneratedBy ECO_0000203 NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_provenance.