Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- 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.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_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." NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_provenance.
- NP324305.RA-rfFQ72hLweqbpzM_Vd3lnp8xbyH5seWPRf1jGSENKY130_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." NP324305.RA-rfFQ72hLweqbpzM_Vd3lnp8xbyH5seWPRf1jGSENKY130_provenance.