Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_assertion description "[We report here on a case of occlusive stroke at young age and hyperhomocysteinemia with homozygous VN (677C to T) variant in the MTHFR gene as well as homozygous D/D (2756G to A) variant in the MS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_assertion evidence source_evidence_literature NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_assertion SIO_000772 11460881 NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_assertion wasDerivedFrom befree-20140225 NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_assertion wasGeneratedBy ECO_0000203 NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP248844.RAZx-idKGg_Yj2WpCt4QZe0gwaiotWUx1XGiP05UgsxGI130_provenance.