Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_assertion> ?p ?o ?g. }
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- NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_assertion type Assertion NP983724.RAaztpSWLIN1MCl-Mx4PKDQ8MtQa0qi9gUX6VDGaEyr2A130_head.
- 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.